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1

Golden, Isaac, and homstudy@netconnect com au. "The potential value of homoeoprophylaxis in the long-term prevention of infectious diseases, and the maintenance of general health in recipients." Swinburne University of Technology, 2002. http://adt.lib.swin.edu.au./public/adt-VSWT20050228.150047.

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Homoeoprophylaxis (HP) is the use of homoeopathically prepared substances to prevent targeted infectious diseases in recipients. Its first use in an epidemic of Scarlet Fever was documented in 1801. It has been used throughout the world since then for both short-term and long-term preventative purposes. The effectiveness and safety of Golden�s long-term HP program using homoeopathically prepared substances to prevent targeted infectious diseases in recipients was tested through two research projects. The effectiveness of the program could not be established with statistical certainty given the limited sample size and the low probability of acquiring an infectious disease. However, a possible level of effectiveness of 90.3% was identified subject to specified limitations. Further research to confirm the effectiveness of the program is justified. Statistically significant results were obtained that confirmed the safety of the program both in absolute terms as well as compared to all other methods of disease prevention studied. It also appeared possible that a national immunisation system where both vaccination and HP were available to parents would increase the national coverage against targeted infectious diseases, and reduce the incidence of some chronic health conditions, especially asthma.
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Goote, Chryso. "A comparison of symptoms derived from a C4 trituration and the materia medica of an existing, well-proven homoeopathic remedy." Thesis, 2011. http://hdl.handle.net/10321/670.

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Dissertation submitted in partial compliance with the requirements for the Masters Degree in Technology: Homoeopathy, Durban University of Technology, 2011.
C4 trituration provings are a somewhat controversial method of uncovering the therapeutic value of homoeopathic remedies. The key advantage of this method over traditional proving methods is that a substance can be proved in a matter of hours, rather than weeks or months. However there is a lack of research to show whether the results of the two methods are comparable. AIM The aim of this study is to establish whether symptoms elicited in a C4 trituration proving are comparable to symptoms produced in traditional provings of the same substance. If a similarity can be demonstrated – even on a single substance – it may encourage further studies to determine the extent to which C4 provings can be used in association with, or instead of, traditional provings as a means of developing homoeopathic remedies. METHOD Ten triturators were recruited from an existing group of experienced triturators to prove an unknown substance. Data were harvested from debriefing sessions and from notes kept by triturators during the sessions, and these were transcribed and converted to rubrics. An unprejudiced repertorisation was undertaken in an (unsuccessful) attempt to identify the substance before unblinding. After the substance was revealed to be Borax, the rubrics from the C4 proving were statistically compared to rubrics associated with Borax in Radar 9.0, the electronic version of the repertory Synthesis: Repertorium Homoeopathicum Syntheticum (2004), which reflects traditional provings of this substance. The statistical comparison of rubrics was performed in SPSS; a Pearson Chi-Square test was applied to establish statistical significance; and a Cramer's V test was used to determine the strength of that association. RESULT The comparison failed to find a significant correlation between the rubrics from the C4 proving of Borax and traditional provings of the same substance. At a chapter level, there were significant associations between symptoms relating to Hearing and Kidneys but, for reasons discussed at length in the report, these results must be treated with circumspection. CONCLUSION While C4 provings are faster than the traditional method, as refined by Sherr, in view of the above findings it cannot be recommended that C4 provings be considered as a means of developing homoeopathic remedies instead of traditional provings, because C4 provings would not produce a complete symptom picture. RECOMMENDATIONS Recommendations arising from the study include that the exercise should be repeated with a different substance and group of provers, preferably with confidential debriefing of participants (as opposed to group debriefing, which is the norm for C4 provings), to verify these findings.
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Surjoodeen, Erosha. "The efficacy of a homoeopathic complex (Carbo Vegetabilis D9, Lycopodium clavatum D9, Nux Vomica D9 and Robinia Pseudoacacia D9) in the treatment of functional dyspepsia." Thesis, 2008. http://hdl.handle.net/10321/347.

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Thesis (M.Tech.: Homoeopathy)- Dept. of Homeopathy, Durban University of Technology, 2008. xxvi, 161 leaves.
The purpose of this placebo controlled study was to evaluate the efficacy of a homoeopathic complex (Carbo Vegetabilis D9, Lycopodium clavatum D9, Nux Vomica D9 and Robinia Pseudoacacia D9) in the treatment of patients suffering from functional dyspepsia; in terms of the patient’s perception of the treatment. It was hypothesized that the patients treated with the complex would respond favorably in terms of the symptoms associated with dyspepsia. In this experimental study the single variable design was used for its ‘before and after with control’. Thirty patients with functional dyspepsia were selected after been screened according to diagnostic criteria identified by the researcher. These patients were divided into two groups according to simple random sampling. Data was collected at the Homoeopathic Day Clinic at the Durban University of Technology. Group one received the homoeopathic complex and group two received a placebo complex. Patients received treatment over a period of six weeks (three consultations). The patients, during each consultation, in the presence of the researcher, completed the Patient Perception Questionnaire. Results were statistically analysed using the FriedmansTest (inter group comparison) and The Wilcoxon signed Rank Test (intra group comparison). When the three questionnaires for each patient were compared it was found that neither the placebo group, nor the experimental group yielded significant improvement. Therefore the results of this clinical trial demonstrated that this homoeopathic complex is not effective in the treatment of functional dyspepsia, when compared to placebo, in terms of patient perception.
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Shabangu, Nondumiso. "The efficacy of a homoeopathic complex (Nux moschata D6, Phosphoricum acidum D30, Helleborus niger D6, Opium D30) in management of excessive daytime sleepiness." Thesis, 2018. http://hdl.handle.net/10321/3050.

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Submitted in partial compliance with the requirements of the Master’s Degree in Technology: Homoeopathy, Durban University of Technology, Durban, South Africa, 2018.
Background : Excessive daytime sleepiness (EDS) is the inclination or compulsion to fall asleep whilst intending to stay awake; it is believed to negatively affect occupational and social functioning and may be a predisposition towards accidents (Hayley et al. 2014), low productivity and interpersonal problems (Fong et al. 2005). Excessive daytime sleepiness is one of the most common sleep-related symptoms and it affects an estimated 20% of the population (Pagel .2009). The causes of EDS are numerous and include intrinsic sleep disorders (e.g. narcolepsy, obstructive apnoea/ hypopnea syndrome, idiopathic hypersomnia), and extrinsic disorders (Banerjee et al. 2004). Sleep deprivation is probably the most common cause of excessive daytime sleepiness. This clinic trial intended to evaluate the effectiveness of a homoeopathic complex (Nux moschata D6, Phosphoricum acidum D30, Helliborus niger D6, Opium D30) in the management of EDS in terms of the Epworth Sleepiness Scale (Johns, 1991) and Stanford Sleepiness Scale (Hoddes et al. 1973). And this randomised, double-blind placebo controlled study also aimed to provide a safe and effective alternative therapy for EDS. Aim of the study : The objective of this study was to determine the efficacy of a homoeopathic complex (Nux moschata D6, Phosphoricum acidum D30, Helliborus niger D6, Opium D30) and placebo in the management of EDS in terms of the Epworth Sleepiness Scale (ESS) and the Stanford Sleepiness Scale (SSS). Materials and Methodology : A sample group of 35 participants was selected voluntarily to conduct the study on basis of the inclusion and exclusion criteria. The participants were than randomly divided into two groups; a treatment group consisting of 23 participants and a placebo group consisting of 12 participants. Each participant had to attend three consultations in total with the researcher over a period of four weeks at the Durban University of Technology (DUT) Homoeopathic Day Clinic. At the first consultation a comprehensive case history (appendix F) was taken and physical examination (appendix E) was performed by the researcher but no medication was handed at that point. At each consultation the participants with the help of the researcher completed the Epworth Sleepiness Scale (ESS), and the seven days’ baseline Stanford Sleepiness Scale (SSS) was handed to the participants at the first and second consultation which the participants completed without the help of the researcher throughout the trial till their last consultation. Results : Results from the two measuring tools were statistically analysed with SPSS version 24.0. the participant’s level of sleepiness improved in both the treatment group and the placebo group. Intra-group analyses of ESS means revealed that both groups improved significantly over time, intergroup ANOVA analysis however revealed no significant differences between the groups. Section analyses however using the Fisher’s Exact Tests did reveal statistically significant differences within certain variables at some points of the study. Intra-group analyses of SSS data revealed no statistically significant change in SSS scores over the three weeks in both the Homoeopathic Complex and the Placebo Groups, as well as the Inter-group Fischer’s Exact tests revealed no statistically significant differences between the groups. Conclusion : Barring a few exceptions described in Chapter 4 & 5 it can be concluded from the results of the study that statistically the Homoeopathic complex (Nux moschata D6, Phosphoricum acidum D30, Helliborus niger D6, Opium D30) was not superior to placebo in the treatment of EDS. The data shows that both the Homoeopathic Complex and the placebo interventions had a positive effect on EDS and were effective in improving the level of excessive daytime Sleepiness. Irrespective of the general lack of statistical significance between groups a closer analysis of the intragroup and inter-group data does reveal a trend suggesting clinical significance in support of the effectiveness of the homoeopathic complex in the treatment of EDS however this needs to be further explored and confirmed in subsequent studies.
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Hamilton, Garatt. "A homeopathic drug proving of Anthropoides paradiseus 30CH with a subsequent comparison to selected avian remedies." Thesis, 2018. http://hdl.handle.net/10321/3047.

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Submitted in partial compliance with the requirements of the Master’s Degree in Technology: Homoeopathy, Durban University of Technology, Durban, South Africa, 2018.
Aim: The aim of this qualitative study was to determine the homeopathic symptomatology that would arise from a homeopathic drug proving of Anthropoides paradiseus 30CH after it was administered to healthy individuals and to compare the homeopathic symptomatology with selected avian remedies. These avian remedies were Corvus Corax, Acridotheres tristis, Peregrine eagle and Geococcyx californianus. Objectives : Objective 1 The first objective was to determine the proving symptomatology of Anthropoides paradiseus 30CH. This was done as a randomized, double blind placebo controlled homeopathic drug proving in the 30th Hahnemannian potency in 30 healthy volunteers of which 6 were on placebo. Objective 2 : To perform a comparative analysis with selected existing remedies, namely Corvus Corax (Raven), Acridotheres tristis (India myna), Peregrine eagle (Peregrine eagle) and Geococcyx californianus (Roadrunner) all in the avian group. Methodology : The homeopathic drug proving of Anthropoides paradiseus 30CH, was conducted as a double-blind placebo controlled randomized trial with thirty volunteers between the ages of 18 and 75 years old. Provers had a full homoeopathic case history and physical exam performed and thereafter they received their symptom recording journals and the test drug or placebo. Twenty-four of the volunteers received the verum powders whilst the remaining six were administered a placebo (ratio of 4:1). The double-blind design was employed; neither the supervisor, researcher nor the provers themselves knew who received the verum or placebo. The provers recorded their symptoms over a 5 week period. Provers began journaling one week before taking the active drug substance or placebo in order to establish their symptom baseline, and continued recording their symptoms for four weeks after having started the active drug or placebo regime. After the 5 weeks of recording their symptoms, the provers attended a follow-up consultation. After all the journals were collected from the provers, the extraction and collation of the data was conducted, and thereafter the data was presented in Materia Medica and repertory formats. The Results: The homoeopathic drug proving of Anthropoides paradiseus produced a variety of symptoms. The main symptoms belonged to both the mental/emotional and the physical sphere. The symptoms of the mental sphere of this remedy included anxiety, disorientation, mood swings and irritability. The characteristic physical symptoms includes polyuria, polyphagia, polydipsia, headaches, muscle pain and spasms, post-nasal drip, hay-fever, and bloating. Other possible uses might be for the treatment of chest pain, nausea and abdominal cramping. The comparative analysis of the selected avian remedies, namely Falco peregrinus, Corvus corax, Geococcyx californianus and Acridotheres tristis, and Anthropoides paradiseus revealed common mental emotional themes of detachment, a drugged or floating sensation and on the physical sphere the group analysis revealed the following common symptoms: numbness, obstruction, dryness and appetite fluctuations. The conclusion : It was discovered that Anthropoides paradiseus 30CH produced symptoms that can be used in the treatment of attention deficit disorder, mood swings, anxiety, pre-diabetes, hay fever, sinusitis, muscle pain and spasms, gastroenteritis and headaches. It was also determined that the remedy, according to the correlating themes, belonged to the AIDS miasm. The conclusion of the group comparison generated the following themes and symptoms: detachment, drugged sensation, restriction, neurological symptoms, obstruction, dryness and appetite fluctuations.
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Ally, Sameer. "The efficacy of a homoeopathic complex (Kalium bromatum 9CH, Natrum muriaticum 9CH, Selenium 9CH, Sulphur 9CH and Thuja occidentalis 9CH) in the treatment of acne vulgaris." Thesis, 2014. http://hdl.handle.net/10321/1059.

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Submitted in partial compliance with the requirements of the Master’s Degree in Technology: Homoeopathy, Durban University of Technology, 2013.
Introduction Acne vulgaris is a common skin condition (disorder of the pilosebaceous duct) which is universal in adolescence. Acne vulgaris can persist into adulthood, with 1% of males and 5% of females requiring treatment until 40 years of age. Aim The aim of this study was to determine the efficacy of a homoeopathic complex (Kalium bromatum 9CH, Natrum muriaticum 9CH, Selenium 9CH, Sulphur 9CH and Thuja occidentalis 9CH), compared to placebo, in the treatment of acne vulgaris. Methodology A total of 37 participants between the ages of 18 and 31 were recruited from the Greater Durban area by means of poster advertisements placed on notice boards in shops, pharmacies, health shops, hospitals, schools, tertiary institutions including Durban University of Technology, and other public areas. Handouts were also left at these areas for people to take home. The final sample consisted of 34 participants due to the drop out of 3 participants. After participants read an information letter (English or Zulu), fulfilled the inclusion and exclusion criteria of the research, were diagnosed as having acne vulgaris by the researcher and completed an informed consent form (English or Zulu) and confidential patient information form (English or Zulu), they were randomly assigned to an experimental (homoeopathic complex) group and a control (placebo) group. In the final sample, the experimental (homoeopathic complex) group consisted of 7 males and 10 females, and the control (placebo) group consisted of 9 males and 8 females. Consultations took place at the Durban University of Technology Homoeopathic Day Clinic, and consisted of 3 consultations, an initial consultation followed by 2 follow-up consultations at 3 weekly intervals. The treatment period for each participant was therefore 6 weeks. A case history was taken and a complete physical examination was performed for all participants. The Leeds counting technique was used to assess and measure the response to treatment. The lesions assessed were the non-inflamed lesions (blackheads and whiteheads), inflamed lesions (papules, pustules, nodules, cysts and deep pustules) and the total number of acne lesions (number of non-inflamed and inflamed lesions combined). The response to treatment was measured in terms of a reduction in the number of non-inflamed, number of inflamed and total number of acne lesions, on the face, over the 6 weeks. SPSS version 20 was used to analyse the data. A p value of < 0.05 was considered as statistically significant. Non-parametric tests were used to analyse the data. The number of non-inflamed, number of inflamed and total number of acne lesions were compared within groups using the Friedman test and between groups using the Mann-Whitney U test. The number of lesions was compared separately for males and females, and also without gender classification. Results In females, the control (placebo) group showed a statistically significant reduction in the total number of acne lesions when compared to the experimental group (p = 0.034). However, as a whole, it was concluded from the results of this study that there was no significant difference in the number of non-inflamed (p = 0.193), number of inflamed (p = 0.290), and total number of acne lesions (p = 0.193) between the experimental (homoeopathic complex) and control (placebo) groups. Both groups showed a similar reduction when compared to each other. Conclusion It was concluded that the homoeopathic complex was not effective in the treatment of acne vulgaris.
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Govender, Saiesh. "A comparison of the effectiveness of two homoeopathic dosage forms of Momordica charantia in the treatment of type 2 diabetes mellitus in patients on metformin." Thesis, 2012. http://hdl.handle.net/10321/753.

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Mini-dissertation was submitted in partial compliance with the requirements for the Master’s Degree in Technology: Homoeopathy, Durban University of Technology, 2012.
It was reported by the International Diabetes Federation (IDF) Diabetes Atlas, in 2003, that a prevalence figure of 3.4% exists for the 24 million South Africans between the ages of 20 and 79, with an expected increase to 3.9% by 2025. Considering that patients with diabetes are at increased risk of cardiovascular disease, blindness, amputation and renal failure it is therefore not surprising that the costs associated with diabetes are estimated to increase worldwide. It is clear that according to the current trends in dietary and exercise practices, South Africa will be affected by the rise in obesity and subsequent diabetes mellitus. It is critical that a concerted effort involving all parties concerned be made to combat this rapidly increasing problem (Rheeder, 2006:20). AIM The purpose of this double-blind, randomized clinical trial was to compare the effectiveness of Momordica charantia homoeopathic mother tincture as compared to Momordica charantia 6CH, in the treatment of type 2 diabetes mellitus in patients on Metformin. METHODOLOGY Thirty patients were recruited and were selected for the study on the basis of inclusion and exclusion criteria. These participants were then randomly and equally divided into two groups. Each participant attended a total of four consultations with the researcher, over a two month period, at the Durban University of Technology (DUT) Homoeopathic Day Clinic. At the commencement of the first consultation, each participant received the subject information letter (Appendix A) for perusal and the informed consent form (Appendix B) to sign. Following this, the researcher took a full, detailed iv case history (Appendix F) and performed a physical examination (Appendix G) of each patient. Participants were required to have a Glycosylated haemoglobin (HbA1C) test performed following the first and fourth consultations. Participants were also required to complete daily Log Sheets (comprising self administered fasting blood glucose readings using issued Bayer Ascensia Elite Glucometers) for the entire duration of the study (8 weeks). SPSS version 18 was used to analyse the data. A p value < 0.05 was considered as statistically significant. The time effect was assessed for intra-group comparison whereas the time x group treatment effect was assessed for inter-group comparison. Means were calculated for both fasting blood glucose and glycosylated haemoglobin for the two respective groups and tabulated in order to describe the data obtained (Descriptive statistics). RESULTS Both groups reflected a statistically non significant decrease in fasting blood glucose levels with no significant differences between the two groups when comparing reduction in fasting blood glucose levels. Group 1 (Momordica charantia homoeopathic mother tincture) reflected a non significant increase in glycosylated haemoglobin (HbA1C) levels while Group 2 (Momordica charantia 6CH) reflected a statistically significant increase over time in HbA1C levels. There were no significant differences between the two groups when comparing reduction in HbA1C levels.
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Mkhize, Pretty Brightness. "A comparison of the efficacy of Syzygium Jambolanum (Java Plum) 6CH and Syzygium Jambolanum (Java Plum) homoeopathic mother tincture in the treatment of type 2 diabetes mellitus in patients on Metformin?" Thesis, 2016. http://hdl.handle.net/10321/1557.

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Submitted in partial compliance with the requirements of the Master’s Degree in Technology: Homoeopathy, Durban University of Technology, Durban, South Africa, 2016,
Background Diabetes mellitus is a metabolic disorder with various aetiologies, characterised by hyperglycaemia, resulting from defects of carbohydrate, fat and protein metabolism due to the deficient action of insulin on target tissues caused by insensitivity to or lack of insulin or both. The long term effects of diabetes mellitus frequently include retinopathy, nephropathy and neuropathy and an increased risk of other diseases such as cardiac, peripheral arterial and cerebrovascular disease. According to the International Diabetes Federation (IDF) 387 million people have diabetes mellitus and this number is predicted to rise to 592 million worldwide by 2035. In 2014 diabetes mellitus caused 4.9 million deaths worldwide and every 7 seconds a person dies from diabetes mellitus. The growing incidence of diabetes mellitus is a worldwide concern because of the increase of economic costs and burden of disease that is due to the cardiovascular complications and the co-morbidities. Objective The aim of this double-blind, randomised clinical trial was to determine the efficacy of Syzygium jambolanum (Java plum) 6CH and Syzygium jambolanum (Java plum) homoeopathic mother tincture on daily fasting blood glucose and glycosylated haemoglobin levels in type 2 diabetes mellitus patients on Metformin® in the treatment of type 2 diabetes mellitus. Material and Method A sample consisted of 24 volunteers selected on the basis of inclusion and exclusion criteria. These participants were then randomly divided into two groups, 13 in the group receiving the homoeopathic potency and 11 in the group receiving the homoeopathic mother tincture. Each participant attended a total of five consultations with the researcher over a period of 14 weeks that included a 2 week baseline period followed by a 12 week treatment period, at the Durban University of Technology (DUT) or Kenneth Gardens Homoeopathic Day Clinic. At each consultation a detailed and comprehensive homoeopathic case history (Appendix D) was taken and a physical examination (Appendix E) was performed by the researcher. Participants were required to fill in a log sheet (Appendix C1 and C2) with their fasting blood glucose readings daily for 14 weeks, which included a 2 week baseline period followed by a 12 week treatment period. Participants were also required to have their glycosylated haemoglobin measurements tested pre- and post-treatment. Results Both groups reflected a statistically significant reduction in fasting blood glucose levels as compared to the baseline. The mean fasting blood glucose level in week 1 was 11.8802 whereas in week 13 the mean blood glucose level was 8.6590 with a p value ≤ 0.05 for the Syzygium jambolanum 6CH group and the mean blood glucose level in week 1 was 9.0338 with a standard whereas in week 13 the mean blood glucose level was 6.8591 with a p value ≤ 0.05 in the Syzygium jambolanum homoeopathic mother tincture. However there was no significant differences between the two groups (Syzygium jambolanum 6CH and Syzygium jambolanum homoeopathic mother tincture), the significance score was 0.623 when comparing reduction in fasting blood glucose levels. Both groups reflected a statistically non-significant reduction in the glycosylated haemoglobin (HbA1C) and there were no significant differences between the two groups when comparing reduction in HbA1C levels. Conclusion Both homoeopathic preparations of Syzygium jambolanum (mother tincture and 6CH) significantly reduce fasting blood glucose levels in patients with type 2 diabetes mellitus. This result suggests that Syzygium jambolanum has beneficial anti-diabetic effects and warrants further investigation.
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Ngoie, Carole Monga. "The efficacy of a homoeophathic complex (Angelica sinensis, Dioscorea villosa 6cH, Matricaria chamomilla 6cH, Viburnum opulus 6cH, and Zingiber officinalis 6cH) compared with homoeopathic similimum (30 cH plussed) in the treatment of primary dysmenorrhoea." Thesis, 2018. http://hdl.handle.net/10321/3082.

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Submitted in partial compliance with the requirements of the Master’s Degree in Technology in Homoeopathy, Durban University of Technology, Durban, South Africa, 2018.
Dysmenorrhoea is the term used to describe painful menstrual cramps, and is the most commonly encountered gynaecological disorder. It affects more than 50% of women of reproductive age, of which 10% to 12% experience severe dysmenorrhoea that interferes with their daily lives by incapacitating them for 1 to 3 days each month. Dysmenorrhoea is estimated to be the single greatest cause of working hours lost by women and school absence in teenage girls (Dawood 2008; Lindeque 2015: 6-9). Primary dysmenorrhoea is defined as painful, spasmodic cramping in the lower abdomen just before and/or during menstrual bleeding, in the absence of any identifiable macroscopic pathology. It is related to increased levels of inflammatory markers such as vasopressin, prostaglandins (PGF2α) and leukotrienes from the secretory endometrium. These induce ischaemia due to excessive prolonged uterine contractions, increased the sensitivity of pain fibres, and cause vasoconstriction (Iacovides, Avidon and Baker 2015: 1-17; Stewart and Deb 2014: 296-302). This double-blinded randomised study aimed to establish the efficacy of a homoeopathic complex (consisting of Angelica sinensis 6cH, Dioscorea villosa 6cH, Matricaria chamomilla 6cH, Viburnum opulus 6cH and Zingiber officinalis 6cH) compared to a homoeopathic similimum in 30cH plussed potency in the treatment of the symptoms of primary dysmenorrhoea, in terms of the participants’ perception of the treatment. Thirty female students, who signed the inform consent forms (Appendices B and D), from the Durban University of Technology were selected based on specified inclusion and exclusion criteria after they underwent an abdominal ultrasound examination (Appendix D) by a gynaecologist. They were randomly divided by means of convenience sampling according to a randomisation sheet into two groups. There were 20 in the experimental group which received the homoeopathic complex, and 10 in the control group which received the homoeopathic similimum. The study took place at the Homoeopathic Day Clinic, located at the Durban University of Technology. It was conducted over a period of three menstrual cycles per participant. The initial consultation took place prior to a menstrual period and the subsequent three follow-ups took place once a month, a week after each menstrual period. During each consultation, a detailed homoeopathic case history was conducted and a physical examination including an abdominal examination was performed. In addition, the participants were required to complete the Moos Menstrual Distress Questionnaire (Moos 1968) (Appendix G) and the Pain Rating Scale (British Pain Society 2006) (Appendix H). SPSS version 23.0 software was used to analyse the data collected from these questionnaires. The quantitative variables across the groups were compared using the Kruskal-Wallis test since the captured data was non-parametric. The one-way analysis of variance (ANOVA) was used to compare intra-group data. Quantitative variables were expressed as a mean ± standard deviation. A p-value less than 0.05 was considered significant. The intra-group analysis using the PRS and the MDQ scales (Appendices G and H) showed statistically significant changes in the subcategories of pain in the simillimum group, while these changes were noticed in the complex group only with the PRS scale, when different follow up mean pain score was compared to that at baseline. The different comparisons and p-values can be found in the Appendix G1. The homoeopathic complex group showed more statistically significant changes in the subcategories of behaviour change, negative affect, and control (Appendix G1); while the homoeopathic similimum also revealed other statistically significant changes in the autonomic response and appetite change subgroups (Appendix G1). The inter-group analysis did not reveal any statistically significant change between the groups, although a decrease in the majority of the various mean scores was observed throughout the study. The study’s results led to the conclusion that both the homoeopathic complex and homoeopathic similimum were effective (Appendix G1) in the treatment of symptoms of primary dysmenorrhoea during various follow-ups, as well as reducing the need for allopathic pain medications in the participants during the study. However that efficacy shown by the presence of statistically significant results could not been maintained throughout the study from the baseline to the third follow-ups, this could be due to the smaller sample size of the participants, the need for a better suited similimum remedy with a higher potency for the control group; or the need for another complex remedy, It was also noted that there was no evidence that one treatment was more beneficial than the other even though a decrease in the mean scores was observed in both groups.
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Wallace, Natasha. "A homeopathic drug proving of Yam ha-Melach 30CH with a subsequent comparison to the materia medica of its constituent minerals." Thesis, 2009. http://hdl.handle.net/10321/512.

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Mini-dissertation submitted in partial compliance with the requirements for the Master's Degree in Technology: Homoeopathy, Durban University of Technology, 2009.
Provings are important to expand known materia medica and advance homeopathy. The Dead Sea was chosen as a substance because it has numerous therapeutic properties in its crude form, making Yam ha-Melach an invaluable homeopathic remedy as the therapeutic properties of a substance is increased during the potentization process. Objective The objective of the study was to investigate the therapeutic potential of Yam ha- Melach 30CH, on healthy provers and to record the signs and symptoms produced, so that it may be prescribed according to the Law of Similars, to those presenting with similar symptoms and further to compare the materia medica of Yam ha- Melach’s constituent minerals with symptoms obtained from the proving of Yam ha- Melach 30CH. Methodology This proving took the form of a randomised double-blind, placebo controlled study. The potency used was the 30th centesimal potency or 30CH. The proving population consisted of a combined project of twenty provers who met the inclusion criteria (Appendix A). Ten percent of the test group (two subjects) received placebo and the rest received Yam ha-Melach 30C (18 subjects). In order for the study to have remained double blind, neither the researchers nor the provers were aware of who received placebo and who received the remedy. Data collection was in the form of a journal kept by each prover, in which their symptoms were recorded daily for a total of five weeks, before, during and after taking the powders. On completion of the proving, data obtained from the journals were analyzed by the researcher for suitability of symptoms for inclusion in the materia medica of Yam ha-Melach. These symptoms were then translated into ii materia medica and repertory language, and a homeopathic picture of the remedy formulated. Data obtained from the case histories and physical examinations (Appendix E) and group discussions were also considered. A comparison between the ‘minimum characteristic syndrome’ of Yam ha-Melach and the symptoms on the mental, emotional and physical planes of each of Yam ha- Melach’s main constituent mineral remedies and their group themes were made, whereby the essential similarities and differences between them were elucidated. The main constituent minerals of the Dead Sea are magnesium chloride, potassium chloride, sodium chloride, bromide and sulphur. The materia medica of Yam ha- Melach’s main constituent minerals therefore included the remedies: Magnesium muriaticum Kali muriaticum Natrum muriaticum Bromium Sulphur The proving symptoms were also compared to the materia medica group themes of the Magnesuims, Kali’s, Bromatums, Muriaticums and the Natrums in Scholten’s Homeopathy and Minerals (Scholten, 1993). Rabinowitz (2008) conducted an analysis of the proving symptoms, comparing the symptoms with existing indications of the Dead Sea’s clinical therapeutic use, in a parallel study of similar methodology. Symptoms were taken from the groups of both studies and included in the materia medica and repertory for Yam ha-Melach. Results The symptoms obtained from the proving had a very definite polarity. On the one side there was depression and loneliness, whilst on the other side there was happiness. This was shown also on the mental sphere, which varied from confusion to mental clarity. iii The main symptoms of this proving were the dreams, especially of war; violence; evil; religion; family and friends. Provers experienced a wide range of symptoms on mental, emotional and physical levels during the study. The main themes were feelings of loneliness and isolation, depression and hopelessness, being emotionally overwhelmed and crying, irritability and frustration, worrying about family and friends, needing affection, paranoia, oversensitivity and mood swings; and the feeling of being relaxed, calm and happy. The polarity continued on the physical level with regards to sleep, energy and appetite. On the physical level provers experienced dehydration resulting in headaches, dry itchy skin, eyes and mouth with diarrhea or constipation as well as nausea and vomiting. Some of the subjects had no appetite while others had an increase in appetite. Provers noted flu and hay fever like symptoms as well as joint and muscle stiffness and pain. Numbness, pins and needles and increased sensitivity were present in the extremities of most provers. Provers noticed pimples and dry patches on skin with severe itchiness and burning all over. Sleep was affected with some provers having difficulty sleeping, waking up all the time and others sleeping like a ‘rock.’ There was either a lack of energy or an increase in energy levels. Some provers had hot flushes and others felt cold and noticed fluctuations of body temperature. There was a general increase in perspiration. Some provers displayed black rashes and black stools. Provers experienced a general aggravation from alcohol. The main cravings were for salty food and coffee. The main aversion was for sweets. There was a general increase in thirst among the prover population. Conclusions The 30CH potency of Yam ha-Melach produced clearly observable signs and symptoms in healthy provers. Comparing the symptoms elucidated from the proving iv of Yam ha-Melach to the materia medica of its mineral constituents attempted to expand and clarify the therapeutic action of the remedy and allowed a better understanding of the similarities and differences between Yam ha-Melach and these remedies that exist in known materia medica. A complete and thorough understanding of Yam ha-Melach and its relationship to these remedies was achieved and contributed to a comprehensive remedy picture and aided in its practical application. The comparison revealed that Yam ha-Melach was most similar to Magnesium muriaticum on mental, emotional and physical planes. Both remedies had similar feelings of aggression, depression, being overwhelmed quickly, dreams of water, anxiety and restlessness, lethargy and similar sensations and complaints on the physical level. This is interesting as the Dead Sea consists of 53% magnesium chloride, 37% potassium chloride, 8% sodium chloride, low concentration of sulfate ions and a high bromide concentration. Magnesium chloride is therefore the main mineral constituent of the Dead Sea.
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Naicker, Dinesha. "An ontological analysis of the visual expression of water based homeopathic remedy, Natrum muriaticum, as droplet glass stain patterns." Thesis, 2016. http://hdl.handle.net/10321/1779.

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Submitted in partial compliance with the requirements of the Master’s Degree in Technology: Homeopathy, Durban University of Technology, Durban, South Africa, 2016.
INTRODUCTION: The idea of the memory of water arose in the laboratory of immunologist, Jacques Benveniste in the late 1980s where his research into allergies took him deeper intotrying to find out how the smallest amount of a substance could affect an organism. He experimented with Homeopathy by using highly diluted antibodies in his basophil degranulation test. He observed that highly dilute biological agents were still able to trigger the relevant biological system. (Thomas, 2007) The memory of water is a controversial topic that requires more research to be properly understood and as such, it is the researcher’s aim to gain insight on the memory of water. METHODOLOGY: The purpose of this study was to examine the effect that the preparation of a Homeopathic remedy (Natrum muriaticum) has on water, as its solvent, using the glass stain analysis as outlined by Kroplin (2001). The possible ability of water to hold and store the memory of its solute, sodium chloride, was investigated. The results would be added to the critical reflection on current literature available. In an experimental double blind study, Kroplin’s glass stain method was used to analyse the following:  The mother solution samples.  The 9CH potency samples (within Avogadro’s constant).  The 30CH potency samples (past Avogadro’s constant).  As well as the water sample used to make the remedy as the control. The above four samples were supplied from the following two manufacturers:  Durban University of Technology (DUT) manufactured by the researcher (appendix 2).  Samples manufactured by one commercial homeo-pharmaceutical company, ParcevalPharmaceuticals (appendix 3). This research aimed to investigate, using homeo-pharmaceutical principles (dilution and succussion), the structural influence of a solute on water after the solution is diluted beyond Avogadro’s constant. Repetition of the 5 experiment in week six aimed to investigate the validity of expiry time proposed by the homeopathicpharmacopoeia. RESULTS:  The stained picture patterns took on a consistent form of a starry night and the ‘stars’ seemed to increase in mass with potentisation suggesting that the homeopathic remedy manufacture process affects the outcome of the water’s form.  Overall consistency in picture patterns between both experimenters suggesting minimal observer effect.  The experiment was repeated to test expiry date and these pictures displayed degradation and thus seemed to offer validation towards homeopathic remedy expiration.  Although abstract qualitative results, a notable difference in water control and potentised water samples offer enough evidence for further investigations.
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Sukati, Behlulile Nonsikelelo Stoppy. "The efficacy of a homoeopathic mother tincture complex (Vitex agnus castus, Melissa officinalis and Valeriana officinalis) in the management of premenstrual dysphoric disorder." Thesis, 2018. http://hdl.handle.net/10321/3060.

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Submitted in partial fulfillment of the requirements for the Degree of Master of Technology in Homoeopathy, Durban University of Technology, Durban, South Africa, 2018.
Research Problem Statement Premenstrual dysphoric disorder (PMDD) is a severe form of premenstrual syndrome (PMS) that involves a combination of emotional and physical symptoms that result in significant functional impairment. PMDD can be debilitating and there are multiple treatment options available, but these are not without side effects. Although complimentary or alternative medicine may be beneficial in treating PMDD, however, there is not enough data available to validate their effectiveness. This study aimed at comparing and determining the efficacy of a homoeopathic mother tincture complex (Vitex agnus castus, Melissa officinalis and Valeriana officinalis) compared to placebo in the management of PMDD. Methodology A sample size of 30 consenting female participants with PMDD who met the inclusion criteria as set out in the Diagnostic and Statistical Manual of Mental Disorders. The duration of the study was three months for each participant. Participants were randomly divided into experimental and placebo groups with three consultations over the study period where Kessler Psychological Distress Scale and Visual Analogue Scale were applied. Non-parametric and inferential analysis of data were performed to analyse and compare the effects of treatment and time on symptoms over the three consultation periods (α.05). Results Results for both scales showed no statistical significance in the interaction between time and treatment. The results showed no statistical differences between the control and experimental group in the management of PMDD. However, the mean value measured in the experimental group were consistently lower than the control. Conclusion The conclusion derived from this study is that the homoeopathic complex studied is not effective in the treatment of PMDD. None of the results showed significant differences between the treatment and the placebo group trials. Further studies are highly recommended in this field.
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Belling, Kym. "The relative effectiveness of the combination of spinal manipulation and Homoeopathic Simillimum in the treatment of chronic mechanical neck pain." Thesis, 2017. http://hdl.handle.net/10321/2569.

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Submitted in partial compliance with the requirements for the Master’s degree in technology in Technology: Homoeopathy, Durban University of Technology, Durban, South Africa, 2017.
Background: According to Picavet and Schouten (2003) the incidence of neck pain is increasing at a greater rate than other spine problems (Hoving et al. 2004). Furthermore, chronic neck pain is a substantial burden to society with chronic neck pain being the fourth leading cause of disability worldwide (Hoy et al. 2014). Chronic mechanical neck pain (CMNP) has been defined as localised, asymmetrical neck pain with restricted range of motion and dysfunctional musculature (Grieve, 1988). Treatments for those suffering with chronic pain, which are non-surgical, appear to be the most beneficial for patients according to Haldeman et al. (2008). Giles and Müller (1999) have stated that spinal manipulation is the most effective method of treating spinal pain on its own. However, the literature suggests that there is benefit in combining manipulation with an “anti-inflammatory type” drug (Crawford 1988; Oberbaum 1998; Serrentino 2003). Many studies have been successfully conducted on Homoeopathic complexes to treat neck pain (Fisher 1986; Bohmer and Ambrus 1992; Hepburn 2000; Soeken 2004) however no study has yet to been carried out on the combination of Homoeopathic Simillimum (single remedy) and spinal manipulation for CMNP. Objective: The aim of this study was to determine if spinal manipulation and Homoeopathic Simillimum in combination are more relatively effective than spinal manipulation alone in the treatment of chronic mechanical neck pain. Methodology: This study was a randomised, blinded placebo controlled quantitative trial with a comparative clinical trial design. Thirty consenting participants with CMNP who met the inclusion criteria were randomly distributed between two treatment groups. Group A received spinal manipulation as well as Homoeopathic Simillimum and group B received spinal manipulation with placebo medication. Each participant received three treatments over a period of a week; with subjective and objective readings taken at every consultation. The subjective tools included the Numerical Pain Rating Scale and Canadian Memorial College of Chiropractic Neck Disability Index. Objective tools included the Algometer and CROM-II Goniometer. All data captured was analysed using SPSS version 24.0. Inferential and non-parametric analysis of the data were also be performed. Results: The results showed that no statistically significant differences were observed between the two groups in terms of subjective and objective measurements. However, there were statistically significant improvements seen in both groups equally in terms of ANOVA subjective and objective measurements i.e. both groups showed improvement. Conclusion: The results of this study concluded that no statistical or clinically significant changes were noticed between the groups and therefore the Homoeopathic Simillimum added no statistical significant improvements in those who received it over those participants who received placebo in the treatment of chronic mechanical neck pain.
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Ngobese, Jabulile Cresancia. "The relative efficacy of homoeopathic Simillimum treatment as compared to psychological counseling (cognitive therapy and behavioral therapy) in the management of Generalized Anxiety Disorder." Thesis, 2006. http://hdl.handle.net/10321/26.

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This double-blind placebo-controlled study investigated the relative efficacy of Homoeopathic similimum treatment as compared to psychological counselling (Cognitive therapy combined with Behavioural therapy), in the management of Generalized Anxiety Disorder (GAD).
Thesis (M.Tech.: Homoeopathy)-Dept. of Homoeopathy, Durban Institute of Technology, 2006 xli, 201 leaves
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Fourie, Daniel Johannes. "Materia Medica III : 'n kurrikulumevaluering." Thesis, 2014. http://hdl.handle.net/10210/11838.

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M.Ed. (Curriculum Studies)
History was made when the Technlkon Natal in January 1989, after approval of the relevant curricula by the Minister of National Education, became the first institution in the Western World to offer an independent tertiary course in homoeopathy. After completion of the five year course, followed by a one year internship, students will be registered with the South African Associated Health Service Professions Board. Homoeopathy originated in Germany when its founder, Samuel Hahnemann (1755 - 1843) rediscovered the principle on which homoeopathy is based - "SimiIia simiIibus curentur": Let likes be cured by likes. In homoeopathy a patient is treated by administering those drugs that could cause similar conditions in a healthy person, to the patient in minute doses. The Materia Medica I I I curriculum is being introduced in 1991. The question posed and researched in this thesis is to what extent the curriculum design complies with curriculum principles. The aim is to evaluate the abovementioned curriculum. To achieve this aim, the following objectives are set:- - to determine the principles involved in the planning and design of a curriculum; - to determine the criteria with which a curriculum should comply; - to determine specific demands and problems posed by the subject; - to establish how and to what extent the Materia Medica III curriculum complies with the criteria and demands; - to make recommendations for the possible improvement of the curriculum. This study is unique in the sense that the curriculum is being implemented this year. Generally accepted models are therefore not applicable and an evaluation instrument has to be developed. The method of enquiry to be followed is mainly a Iiterature study and structured interviews wiII also be conducted.
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Weston, Marion. "A group analysis evaluation of the class Arachnida in terms of known materia medica." Thesis, 2010. http://hdl.handle.net/10321/575.

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Dissertation submitted in partial compliance with the requirements for the Master's Degree in Technology: Homoeopathy, Durban University of Technology, 2010.
Two centuries ago it was possible to practice with only 100 remedies. Today with the constantly expanding materia medica, complexity itself tempts the homeopath to remain inside this range of remedies. It is due to the pioneering work of authors like Scholten (1993) and Sankaran (2005) that the vast materia medica of today can be summarized and understood through a method like group analysis which links naturally related substances via their common symptomatology. This not only offers new aspects to well known remedies, but highlights the smaller, not so well known remedies, resulting in a more comprehensive understanding of the materia medica. Relatively few homeopathic remedies derived from the Araneae order are extensively utilized for the homeopathic treatment of patients. Therefore the spider remedies represented in the literature of Mac Rep computer program® were subjected to the group analysis method in order to extend the overall knowledge of this particular group of homeopathic remedies. The spider remedies were first analyzed in terms of their quantitative representation in the repertory (amount of rubrics) and then a sample group was chosen. This selection was screened for common sensations using the above mentioned computer program. The significance of a common sensation was confirmed by cross-checking the materia medica of all16 homeopathic spider remedies listed in Mac Reference® computer software for its occurrence. The findings were interpreted within the backdrop of the established animal characteristics of homeopathic remedies (Sankaran, 2005:24-31). The primary sensations extracted and confirmed in the rest of the Araneae group were stinging, stitching, shooting, sensitive, sore, cold, faint, paralytic, twitching and full. Significant synonyms of the first order analysis were heaviness, spasm, cramp, numbness and weakness. Second order and third order analysis not only provided symptoms of the mind, but led to the proposed themes common in spider remedies. The majority of themes like hyperactivity, restlessness, increased sexuality, impulsive violence and aggression, the periodicity of complaints, heightened sensitivity to music and the love for dancing are comparable to Mangliavori’s (2004) clinical findings and to Sankaran’s (2005) proposed spider characteristics. A miasmatic differentiation of each member of the sample group was performed according to Sankaran’s extended miasmatic model (2005:7). Araneus diademus was found to belong to the sycotic- as well as malarial miasm, Latrodectus hasseltii to the syphilitic-, Loxoceles reclusa to the leprous- and Tarentula hispanica and Theridion curassavicum to the tubercular miasm. Pathological tendencies of the Araneae remedies were found to involve the nervous system, eyes, heart, muscular – skeletal system, sexual organs and the mind. Examples of diseases common in Araneae remedies were found to be: mental disorders like anxiety neurosis, ADHD, depression, mania, sexual disturbances, STD’s, neurological disorders, angina pectoris, myocardial infarction, spinal irritation, migraines, meningitis etc. The results of this research were found to support group analysis methodology as outlined by Sankaran (2005). However additional knowledge drawn from Sankaran’s 2008) most recent research into animal remedies and from the natural history of spiders was necessary to be able to interpret the results correctly and to illustrate an in-depth picture of the common characteristic features of the Araneae remedies.
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Naidoo, Keshia. "A double blind placebo controlled proving and comparative material medica of Ubiquinone." Thesis, 2015. http://hdl.handle.net/10321/1413.

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Submitted in partial compliance with the requirements for the Master’s Degree in Technology, Department of Homoeopathy, Durban University of Technology, Durban, South Africa, 2015.
INTRODUCTION Homoeopathy is based on the law of similars meaning the medicine that produces symptoms in a healthy individual will cure the same symptoms in a sick individual (Sankaran, 1991:5). AIM Conducting a proving on Ubiquinone 30CH will lead to an establishment of its therapeutic potential through the application of the law of similars thus adding to the Materia Medica and advancing Homoeopathy (Vithoulkas, 2002). It was hypothesised that the 30CH potency of Ubiquinone would clearly produce observable signs and symptoms in healthy prover’s. It was further hypothesised that a comparison of Ubiquinone to those remedies yielding the highest numerical value and total number of rubrics on repertorisation of the proving symptoms would elucidate differences and similarities between Ubiquinone and other Homoeopathic remedies to clarify its therapeutic indications. It was hypothesised that in this manner a better understanding of Ubiquinone and its relationship to other Homoeopathic remedies would be gained. Methodology The proving of Ubiquinone 30CH was a randomised, double blind placebo controlled study, using the 30th centesimal potency and a total of 26 participants who met the inclusion criteria. Each prover was provided with a journal to record their symptoms daily. The data extracted from the journals were added to the case histories and physical examinations to compile a proving profile. The identity of the substance was revealed and the information was correlated after completion of the proving. The symptoms found were translated into Materia Medica and repertory language. Once the proving was concluded, a comparison to the remedies yielding the highest numerical value and total number of rubrics on repertorisation - which is the technique of using a repertory to identify the Homoeopathic medicines whose Materia Medica corresponds most closely to the clinical picture of the patient and from amongst which a simillimum may be chosen (Swayne, 2000:183) - was compared to the proving symptoms. Results The remedy’s main influence was on the mental and physical state. The most prominent symptoms seen in the mental sphere were extreme irritability and exhaustion. There was a sense of emotional fragility with a desire to be alone. On the physical side, headaches were common and weakening pains of the extremities were experienced. It can be concluded that the 30CH potency of Ubiquinone, if used precisely according to Homoeopathic principles, can be applied to a clinical setting, as the extensive range of symptoms produced during the proving suggests an equally wide array of application of the remedy Ubiquinone. Conclusion One of the downfalls of Homoeopathy is the limited number of provings being done, (Vithoulkas, 2002). Vithoulkas (2002:143) maintains that in order for Homoeopathy to advance, it is necessary to perform provings on new substances to expand the Homoeopathic armamentarium. Increasing the number of remedies in the Materia Medica facilitates greater accuracy and individualisation when treating patients (Wright, 1999). According to Herrick (1998) numerous cases cannot be solved because many of the most important remedies have not yet been developed. The purpose of this study was to increase the knowledge of drug substances due to the limited amount of information in our current Materia Medicas, by investigating the therapeutic potential of Ubiquinone 30CH. The investigation supported the hypothesis that Ubiquinone would produce clearly observable signs and symptoms in healthy volunteers. It is essential that the proving symptoms be verified and expanded through clinical use and with further proving of Ubiquinone in various potencies so that it becomes a well utilised remedy in the future.
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Harkhu, Nershada. "A group analysis evaluation of existing avian (bird) homoeopathic remedies in terms of known materia medica." Thesis, 2011. http://hdl.handle.net/10321/661.

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Dissertation submitted in partial compliance with the requirements for the Master’s Degree in Technology: Homoeopathy, Durban University of Technology, 2011.
Until recently homoeopathic remedies have been studied and understood by considering each remedy in isolation (Scholten, 1993). In the last few years a new method of understanding homoeopathic remedies, called group analysis, has emerged (Sankaran, 2002). This method involves an understanding of remedies in terms of characteristics common to a group of related remedies (Leisegang, 2007). Remedies are grouped according to natural classifications. Using the information available in computer repertories, searches are systematically performed to identify rubrics which are common within the group. This type of data analysis yields common characteristics which can be applied to lesser understood groups of remedies. This study was an investigation of the common characteristics of the remedies from the Class Aves, using the method according to Sankaran. The investigation was carried out by applying the group analysis method to the available data. Remedies from the Class Aves are relatively new additions to the materia medica, with the first of these proved in 1995. There is relatively little information available about this group and thus group analysis would be a valuable method of understanding these remedies (Fraser, 2009). A search was performed to determine which bird remedies were best represented in the repertory program iv Radar 10. Based on these results the sample group was selected. The rubrics of these remedies were then analysed to determine common sensations within the group. These sensations were then defined and synonyms were determined. These common sensations were then confirmed by searching for the keywords and synonyms in the available data. Second and third order analyses were performed based on the results. The resultant sensations were also compared with those proposed by Shore (2004) and Fraser (2009), to determine whether these theories on bird characteristics are consistent. Pathological tendencies of the Class Aves were found to involve the throat, female reproductive area, eyes and vision, skin, musculoskeletal system and mental disorders. Clinically there was strong indication for these remedies in cases of depression and anxiety, acne and dermatitis, dysmenorrhoea and disorders of vision such as blurred vision and eyestrain. The results of this study appeared to confirm the validity of theories on group analysis according to Sankaran (2002). The results further confirmed many of the characteristics attributed to the bird remedy group by Shore (2004) and Fraser (2009). Several new common characteristics of remedies from the Class Aves were deduced from the results of the analysis. The study also produced a proposed vital sensation and showed evidence linking several sensations in the process of reaction to the vital sensation.
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Sanjit, Rajeshree. "A repertorial comparison of the proving of a homoeopathic complex to the rubrics of the constitutent parts." Thesis, 2016. http://hdl.handle.net/10321/1780.

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Submitted in partial compliance with the requirements of the Master’s Degree in Technology: Homoeopathy, Durban University of Technology, Durban, South Africa, 2016.
Aim The purpose of this research study was to compare the similarity and differences of the rubrics from a proving of a homoeopathic complex (Cinnabaris 12CH, Hydrastis canadensis 12CH and Kalium bichromicum 12CH) in order to establish whether the symptoms are similar to the individual constituents, or whether a new remedy is produced when individual remedies are combined. The research questions addressed by the study were: 1) Will the twelfth centesimal potency (12CH) of the homoeopathic complex produce clearly observable signs and symptoms in healthy provers? 2) Will the majority of signs and symptoms of the complex be similar to those of its constituent parts? Methodology The proving was a randomised double blind placebo controlled study involving 20 participants who met the inclusion and exclusion criteria. The provers were randomly assigned to either a verum (80%) or placebo group (20%). Provers recorded their symptoms in their journals for one week prior to administration of the proving complex in order to establish a baseline for comparison. The proving complex was in form of lactose granules dispensed in lactose powders. Provers were given six lactose powders, one powder to be taken sublingually three times a day or until symptoms occurred. The provers recorded all mental or physical symptoms experienced in their journals. Once the proving was completed the journals were collected and symptoms derived from the recordings were collated and analysed. This information was converted to materia medica and repertory format. The researcher then analysed each rubric in order to establish if any or all of the three remedies of the complex appeared in that rubric. This comparison reflected the number of rubrics that contained the individual remedies of the complex. In this way the researcher established the rubrics that were unique to the complex as a whole. vi Results A total of 337 rubrics were produced by the proving. The analysis of rubrics showed that 216 rubrics did not contain any of the three remedies; 72 rubrics contained at least one of the three remedies; 29 rubrics contained two of the three remedies; and 20 rubrics contained all three remedies. Eighteen new rubrics were identified. In analysing the symptoms elucidated, a definite polarity between symptoms was noted, including within the same prover. This was the case with mental and physical symptoms. A vast range of symptoms was produced, spanning 29 sections of the repertory, with the majority being physical, related to headaches were quite common amongst provers, pain in the abdominal region, pain in the extremities, eye symptoms such as lachrymation and pain, pain in the throat, chest and neck, skin eruptions. Sinusitis or rhinitis symptoms such as nasal itching, sinus congestion, nasal discharge and sneezing were observed. A significant change in appetite and thirst was seen. The main regions that had an affinity for the complex were the head, abdomen and extremities with pain as the main symptom. Conclusion The substance did produce signs and symptoms in the provers, so Research Question 1 was answered with a “Yes”. Only a small proportion (0.05%) of the rubrics from the proving contained all three constituent remedies, therefore Research Question 2 was answered with a “No”. The results show that although the proving symptoms shared a small degree of similarity to the constituent remedies, the complex as an entity formed its own individual picture.
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Singh, Varuna. "The use of pilocarpus jaborandi in the treatment of emotional palmar hyperhidrosis." Thesis, 1994. http://hdl.handle.net/10321/1976.

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A dissertation submitted in partial compliance with the requirements for the Master's Diploma in Technology: Homoeopathy, Technikon NataI, 1994.
The efficacy of Pilocarpus Jaborandi in the management of emotional palmar hyperhidrosis was studied. It was hypothesised that this homoeopathic drug would cause a significant decrease in sweat production rates. The study was double blinded and consisted of thirty treated patients, with fifteen patients in group and fifteen patients in the the placebo group. Patients were chosen by convenience sampling with no specifications of age or sex. The treated group received Pilocarpus Jaborandi 9 CH, and were instructed to take five pills on waking everyday for ninety days. The other group received a placebo also for ninety days. Quantification of the first day, on ninetieth day of sweat production was done on the forty-fifth day and treatment, by means of on the sweat collection tests. In each test sweat was
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Rautenbach, Hanli. "A study on the effect of a complex formula consisting of homoeopathic Thuja occidentalis DI and Baptisia tinctoria mother tincture on circulating leukocytes." Thesis, 2014. http://hdl.handle.net/10210/11492.

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M.Tech. (Homoeopathy)
Baptisia tinctoria and Thuja occidentalis are reported to be immunostimulants, and thus have an effect on white blood cells. Little formal research has been done to demonstrate their effects on the different white cell populations. The purpose of this study was to determine the effects of these substances on the circulating leukocytes, and to compare these effects to a placebo. An initial full blood count was conducted to establish a baseline level for each subject. The subjects were required to take 18.75 millilitres of the medication or placebo in split doses over a three-hour period. Thereafter, a second full blood count was taken at one-hour intervals. The medication appeared to cause an increase in the lymphocyte count, thus suggesting a possible indication for viral infection. There was an increase in both groups of the total WBC count as well as in the lymphocyte count, raising the question of what substance actually caused these changes to occur. Expansion of this study, including using a larger sample size and longer test period, may be required to validate these results.
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Power, Sean Michael. "An appraisal of homoeopathic quinquagenimillesimal potencies of plumbum metallicum and stannum metallicum by means of nuclear magnetic resonance spectroscopy." Thesis, 1999. http://hdl.handle.net/10321/2697.

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Dissertation submitted in partial compliance with the requirements for the Master's Degree in Technology: Homoeopathy, Technikon Natal, 1999.
The purpose of this study was to investigate the Nuclear Magnetic Resonance spectra of samples of LM6; LM14 and LM22 homoeopathic quinquagenimillesimal (LM) potencies of tin (Stannum metallicum), lead (Plumbum metallicum) and two lactose based controls: one control which is prepared by the means of potentisation and one control prepared without the means of potentisation. It was hypothesised that in terms of the effect of different substances (Stannum metallicum and Plumbum metallicum, and the lactose controls) and of different dilutions (LM6, LM14, LM22) of these substances that significant differences exist between the chemical shift and relative integration values of the CH3, CH2, OH and H20 signals of these homoeopathic substances.
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Ross, Ashley Hilton Adrian. "An appraisal of homoeopathic proving methodology as a bridge between the indigenous and rationalist-scientific understandings of medicinal plants : the case of Strychnos henningsii." Thesis, 2011. http://hdl.handle.net/10321/696.

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Submitted in fulfillment of the requirements of the Degree of Doctor of Technology: Homoeopathy, Durban University of Technology, 2011.
Aim This study sought to appraise homoeopathic proving methodology as a bridge between the indigenous and rationalist-scientific understandings of medicinal plants through a detailed exploration of the relationships existing between data derived from respective paradigmatic explorations of a single African traditional medicinal plant, Strychnos henningsii [Red bitterberry]. Methods The data derived from the implementation of a triple-blind, placebo-controlled homoeopathic proving methodology, on 32 healthy human subjects (50 percent placebo), using the bark of Strychnos henningsii in the 30CH potency, were evaluated for internal consistency and coherence, and subsequently compared to data derived from a phytochemical analysis of the crude bark sample, and translated data derived from semi-structured mothertongue interviews of eight Zulu traditional healers. The proving data took the form of subjective journal data and the results of four objective blood measures of erythrocyte sedimentation rate (ESR), redand white blood cell indices, and liver functions. The subjective data were evaluated in terms of defined inclusion criteria and presented in standard materia medica and repertory formats, and tabulations of objective data were subjected to independent statistical analysis, using repeated-measures ANOVA and profile plots. The crude bark sample was analysed in terms of the presence of strychnine and other indole alkaloids, using highperformance liquid chromatography-mass spectrometry, and interview data related to the indigenous understanding and application of Strychnos henningsii within the traditional African medical paradigm, were audiovisually recorded, collaboratively translated, and independently verified. ABSTRACT iii Qualitative data processing and analysis was effected with the aid of NVivo® software, and a range of comparative analyses were effected with the aid of Radar® homoeopathic software, materia medica references and the Mappa Mundi elemental theory model. Results The proving yielded 581 subjective symptoms, covering a broad range of physical and mental disease manifestations, and nine statistically-significant treatment effects within the objective data set. These included elevation of ESR and changes in two red blood cell indices, four white blood cell indices and two liver function indices. The two proving data sets were demonstrated to show high levels of correlation, although these correlations were not demonstrable for all provers. The phytochemical analysis confirmed the presence of between two and five strychnine-related compounds (excluding strychnine itself), and the field interview data served to confirm all except two documented traditions of use, as well as identifying a number of novel indications and application of Strychnos henningsii bark. The comparative analyses demonstrated the integrity of homoeopathic proving methodology as a mode of scientific investigation, and significant and widespread overlaps of proving symptomatology with both the pharmacology and toxicology of strychnine, and the physical and metaphysical understanding and application within the traditional African medical paradigm. Conclusions Homoeopathic proving methodology was discussed in terms of the evident degree of overlap with the indigenous and rationalist-scientific paradigms, and the incomplete nature of the homoeopathic ‘totality’. A number of recommendations were made for future cross-paradigmatic research.
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Ramnarayan, Sumir. "A double blind placebo controlled homoeopathic proving of Malus domestica 30CH, with a subsequent comparative analysis according to the doctrine of signatures." Thesis, 2014. http://hdl.handle.net/10321/1060.

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Submitted in fulfillment of the Master’s Degree in Homoeopathy, Durban University of Technology Durban, 2014.
The purpose of this research study was to determine any therapeutic significance of Malus domestica (domestic apple) in the potentised, homoeopathic form and to contribute this information to the body of the homoeopathic materia medica. It was further hypothesised that some proving symptoms experienced by the provers during the research study would show a resemblance to unique characteristics of the plant in terms of its natural appearance and cultural references. This involved a detailed doctrine of signatures analysis of Malus domestica based on an extensive literature review. Combining a proving research study with comparative analysis to the doctrine of signatures helped to clarify and verify the remedy’s potential therapeutic value. Methodology This homoeopathic proving was carried out in the form of a double blind placebo controlled study of Malus domestica 30CH with a total of 30 provers. The prover sample was randomly divided into two groups: 24 provers (80%) into the verum group and the remaining six provers (20%) into the placebo group. The provers were unaware of either the proving substance or the potency used. Participants were required to record their mental, emotional and physical status’ one week prior to administration of the proving powders as a form of control for comparison of symptoms post administration of the proving remedy. Thorough physical examinations and case histories of each prover were taken prior to and after the proving period. Provers ingested one powder three times a day for three days and recorded their symptoms daily in a journal. The duration of the proving period spanned five weeks. During this period researchers were in constant contact with all participants. Once the proving period was complete, all journals were gathered and the information therein translated into materia medica and repertory format so as to develop the remedy picture of Malus domestica 30CH. A comparison between the symptomatology produced in the provers and the doctrine of signatures was then performed. Results A wide range of symptoms were documented by the provers. The results revealed an affinity to the mental plane – the most striking being the theme of being disconnected and separated from others in the environment as well as within one’s self. Marked polarities were depicted as follows: Anger/irritability vs. calmness/tranquility; Depression/sadness vs. cheerfulness; Confusion vs. concentration/clarity of mind; Connection vs. disconnection. Physically, symptoms concerning the extremities were numerous, with provers describing symptoms of their limbs being disconnected/separated as well. Head symptoms were also numerous as provers described a wide range of headaches, as well as headaches that were associated with eye symptoms. Abdominal symptoms manifesting as cramping associated with diarrhoea and, in some cases, constipation were documented. Dizziness associated with the sensation of the head floating was common as well. Numerous themes arising from dreams were recorded by provers, with a clear affinity to family members as well as dreams of social gatherings and banquets. Provers dreamt of family members placed in precarious situations wherein the lives of their loved ones were at risk, whilst the emotion of guilt was expressed in certain dreams regarding parties and banquets. The comparison between the homoeopathic drug proving of Malus domestica 30CH and the doctrine of signatures brought many similarities to light, with most of these similarities relating to the mind, extremities and head. Conclusion As hypothesised Malus domestica 30CH produced clearly observable symptoms in healthy provers. On comparison, the proving remedy and the doctrine of signatures brought many parallels to light – the majority of which related to the mind, extremities and head. To gain a complete remedy picture of Malus domestica it is imperative that further research into the symptomatology of different homoeopathic potencies be conducted.
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25

Kasiparsad, Suraj Vishal. "A group analysis of the Salicaceae plant family of homoeopathic remedies in terms of known materia medicae." Thesis, 2012. http://hdl.handle.net/10321/752.

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Dissertation submitted in partial compliance with the requirements for the Master’s Degree in Technology: Homoeopathy, Durban University of Technology, 2012.
Introduction: This study aimed to apply the methodology of group analysis, as proposed by Sankaran, to an under-represented and poorly-understood biological class. The intention of the study was to extend the group understanding of the biological class, with a view to more notable utilization of the individual members of the class as therapeutic substances. The Salicaceae Family was to the knowledge of the researcher, under-utilized in homoeopathy and was expected to have a much larger scope of use than is current. Methodology: The family, Salicaceae, was classified taxonomically. Secondly, an extraction of all rubrics pertaining to the Salicaceae family was done using the Radar® repertory program. Those rubrics that contained at least two remedies from the Salicaceae Family were retained and the rest were eliminated. A search of Encyclopaedia Homoeopathica® and other resources was utilized to derive common sensations, reactions to sensation, and to classify the remedies miasmatically. Results: The primary sensation was a burning sensation, with heat or a sensation of being burnt, which was confined primarily to the respiratory, genitourinary and gastrointestinal system. The next sensation, which was on the physical level, was of a stinging sensation, which may be interpreted as either a tingling or a prickling sensation. This sensation was found to be mostly confined to the skin. Another sensation was a feeling of being alone, in isolation, detached from surroundings, or being forsaken. Passive reactions included numbness, inflammation, tearfulness, trembling and crying. Active reactions were restlessness, irritation and wanting to sneeze. Miasmatically the task was a challenge, as the researcher found materia medica to be lacking in certain remedies. However many of the remedies were found to be Acute, Sycotic, Malarial or Leprous. v Conclusion: The Salicaceae Family had an affinity for all orifices, with many pathological tendencies occurring throughout the gastrointestinal, genitourinary and respiratory system. The researcher felt that the Group analysis of remedies was a powerful tool that can assist in a homoeopathic prescription. It gave great insight to the Salicaceae Family, and exposed the researcher to the lesser known remedies.
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26

Morris, Catherine Anne. "A homoeopathic drug proving of the fungus Pycnoporus sanguineus." Thesis, 2002. http://hdl.handle.net/10321/1960.

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Dissertation submitted in partial compliance with the requirements for the Master's Degree in Technology: Homoeopathy, Technikon Natal, Durban, 2002.
The fungus Pycnoporus sanguineus was selected for this research project because of its similarity in appearance to a human kidney. It was initially thought that a connection to the Doctrine of Signatures could be proved, however, this was not the ultimate purpose of this research project. The purpose of this placebo-controlled investigation was to determine the effects of the thirtieth centesimal (30CH) potency of Pycnoporus sanguineus on individuals of average health; in order to discover the totality of symptoms produced by the remedy so that it may be prescribed according to the law of similars, as required by Homoeopathic science. It was hypothesised that this study would produce a list of symptoms associated with this substance, Pycnoporus sanguineus, which, can then be used Homoeopathically (according to the totality of symptoms produced by the drug so that it may be prescribed according to the law of similars) in the treatment of disease where no other remedy has yet acted precisely and thus be able to cure a class of cases that until then could only have been partially covered by existing remedies (Sherr 1994:58). This Homoeopathic drug proving of Pycnoporus sanguineus 30CH took the form of a double blind, placebo controlled trial on 30 subjects who met all the inclusion criteria. Fifty percent (15 of the 30) of the subjects received placebo in a randomised fashion, so that neither the provers nor the researcher knew who was receiving placebo or verum. As an added control measure, the provers were unaware of the substance, which they were proving or in which potency it was being proved. The study design consisted of two groups: one control group with placebo controls and the other experimental group, which also has intraindividual controls in which the prover serves as his or her own control i.e. the recorded state of the prover prior to the administration of the proving substance served as a control or baseline for comparison to the prover under the influence of the proving substance. (Stephenson 1960; Vithoulkas 1986:150).
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27

Naidoo, Nerisha. "A doctrine of signatures-based evaluation of the results of a triple blind proving of Strychnos henningsii 30CH." Thesis, 2014. http://hdl.handle.net/10321/1061.

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Submitted in partial compliance with the requirements for the Master’s Degree in Technology: Homoeopathy, Durban University of Technology, 2013.
The proving study of Strychnos henningsii 30CH was primarily conducted to extract as many symptoms as possible from healthy provers to create a Homoeopathic picture of the drug. This would allow practitioners in clinical practise to prescribe Strychnos henningsii 30CH based on the Law of Similars. The second part of this study was to assess the symptoms produced, and thereafter determine the relationship to the natural history of the Strychnos henningsii plant as it relates to the Doctrine of Signatures. Methodology The Homoeopathic drug proving of Strychnos henningsii 30CH took the form of a mixed-method triple-blind, placebo-controlled study. The proving population consisted of a minimum of 32 subjects who met all the inclusion criteria. The proving was conducted by 4 M.Tech.Hom students, under the supervision of the principal researcher. The 32 provers were randomly divided into four equal groups of eight provers, with each group supervised by one of four M.Tech.Hom student researchers. Nine powders each of the respective test substance (verum or placebo) was randomly assigned by an independent clinician to 32 prover numbers (16 verum and 16 placebo). Randomisation was conducted by an independent clinician who was unaware of the proving substance. The physical and behavioural symptoms that were noted by the provers were extracted from their prover journals, case-histories and post-proving group discussions. This was then written up into Materia Medica and Repertory format and graded accordingly. Once this proving data was captured it allowed for the application of the Doctrine of Signatures. During this analysis, similarities were compared between the behaviour of the patient and the behaviour of the substance in nature, which indicated the therapeutic action of the plant. The main characteristics used to link the Strychnos henningsii plant in its natural state to the Homoeopathic remedy developed was the plants habitat, kingdom, toxicity, structure, Anthroposophy and Vibrational therapy. By applying the Anthroposophical and vibrational therapy view, it allowed the researcher to establish a more holistic approach. Results A broad spectrum of symptoms was obtained which resulted in the formation of 876 rubrics. The areas that Strychnos henningsii had a profound affinity for were the mind which yielded 170 rubrics, head (76 rubrics), extremities (82 rubrics), dreams (91 rubrics) and the generals (80 rubrics). These rubrics were used in the evaluation of the Doctrine of Signatures. The sensation of heat, dryness and burning appeared to be an integral part of the manifestation of symptoms in this proving study which correlated to the habitat of the plant in its natural environment. Many mind themes were noted, but in particular emotional sensitivity was one of the major themes. Sensitivity is the Plant Kingdom’s key sensation in general. The remedy was prepared using the bark of the plant which contained high levels of the alkaloid strychnine. This reflected in the provers symptoms (itching, skin eruptions, cramps, stiffness, tingling). The structure, colour, mode and speed of growth were all factors which yielded satisfactory comparative results. Chakras, Colour Therapy and Anthroposophy allowed the researcher to apply a more dynamic scientific methodology. This tied in well with the Doctrine of Signatures and essentially provided a broader understanding of the remedy. Conclusion The hypotheses of this study were largely validated by the symptoms produced and analysis conducted, after applying the scientific methodology. The Doctrine of Signatures evaluation helped to reveal the intrinsic nature of Strychnos henningsii, further highlighting the underlying themes in the remedy and explained certain symptoms in more detail and finally distinguished between the behaviour of the patient and the substance in nature aiding us with a better understanding for clinical practise. It is important to note that recommendations have been made for future provings.
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Wayland, Lauren. "A homoeopathic drug proving of the plant Peucedanum galbanum with a subsequent comparison to those remedies yielding the highest numerical values and total number of rubrics on repertorisation of the proving symptoms." Thesis, 2007. http://hdl.handle.net/10321/368.

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Thesis (M.Tech.: Homoeopathy)-Dept. of Homoeopathy Durban University of Technology, 2007. 250 leaves
This research study was conducted to elucidate the total symptomatology that the plant Peucedanum galbanum in the thirtieth centesimal potency would produce on healthy individuals so that it may be prescribed according to the Law of Similiars. A further aim of the investigation was to compare this remedy to other remedies yielding the highest numerical values and total number of rubrics on repertorisation of the proving symptoms. Wagner (2007), in a concurrent study, analysed the proving results of Peucedanum galbanum in relation to the doctrine of signatures. It was hypothesised that Peucedanum galbanum 30CH would produce recognizable signs and symptoms in healthy provers, and that the comparative study of this remedy would highlight the differences and similarities between remedy symptoms and thus confusion as to indication is eliminated, plus a fuller understanding of the remedy and its relationship to other remedies is gained.
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29

Vogel, Alta. "A group analysis evaluation of the class Insecta in terms of known materia medica." Thesis, 2007. http://hdl.handle.net/10321/33.

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Thesis (M.Tech.: Homoeopathy)-Dept. of Homoeopathy, Durban Institute of Technology, 2007 ix, 153 leaves
Group analysis of homoeopathic remedies is a relatively new methodology, linking naturally related substances via their common symptomatology. At its very basic level of understanding, it is an attempt to identify a mechanism for understanding groups of related remedies according to the natural classification of various sources used in homoeopathic practice (Scholten, 1993). This not only offers new aspects to well known remedies, but illuminates the smaller, less well known remedies, resulting in a more comprehensive and rounded understanding of the materia medica
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30

De, la Rouviaere Lize. "A homoeopathic drug proving of Hemachatus haemachatus, with a subsequent comparison of the proving symptoms with that of other snake remedies used in homeopathy." Thesis, 2008. http://hdl.handle.net/10321/436.

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Mini-dissertation submitted in partial compliance with the requirements of the Master’s Degree in Technology: Homoeopathy in the Faculty of Health Sciences at the Durban University of Technology, 2008.
The aim of this study was to elicit and document the effects, in the form of signs and symptoms produced in relatively healthy volunteers, of the venom of Hemachatus haemachatus, prepared in accordance with the methods set out in the homoeopathic pharmacopoeia. These signs and symptoms form the indications for the prescription of the remedy, according to the homoeopathic Law of Similars. A further aim of this study was a comparative analysis of symptoms produced by Hemachatus haemachatus 30ch with existing remedies derived from snake venom used in homeopathy, with the aim of highlighting the similarities and differences between them. The homoeopathic drug proving of Hemachatus haemachatus 30ch took the form of a double-blind, placebo controlled trial. The proving population consisted of 30 healthy subjects who met with the necessary inclusion criteria (Appendix B). Eighty percent (24 subjects) served as the experimental group, receiving the active verum in a randomised manner, while twenty percent (6 subjects) formed the placebo group, receiving non-medicated placebo powders in a randomised manner. Provers were unaware of either the nature or potency of the substance. Verum and placebo were indistinguishable from each other, and neither researcher nor volunteers knew who received verum and who received placebo. Intra-individual control was achieved through a pre-proving observation period of a week’s duration, during which provers recorded the signs and symptoms of their normal state. This symptom picture served as a baseline for comparison with symptoms noted after administration of the remedy. Verum and placebo were dispensed in the form of six powders to be taken sublingually three times a day for a period of two days, or until the onset of symptoms. Data was primarily collected in the form of a diary or journal kept by each prover in which they recorded symptoms on a daily basis. Provers were closely monitored by the researchers during this period. Data collected by the researchers during daily telephonic contacts, as well as during the pre-proving consultation, was also considered. Information obtained from the journals was then assessed by the researchers for suitability for inclusion in the materia medica of Hemachatus haemachatus. The data did not require statistical analysis. In a concurrent study of similar methodology, Cahill (2008) conducted a comparison of the symptom complex produced in the proving of Hemachatus haemachatus, with other homeopathic remedies which scored highest on repertorisation. Symptoms from both studies were collated and included in the materia medica and repertory of Hemachatus haemachatus. The investigation supported the hypothesis that Hemachatus haemachatus would produce clear and observable signs and symptoms in healthy proving volunteers. During the course of this study provers experienced a wide range of mental, emotional and physical symptoms. The highest number of symptoms was produced on the mental and emotional level. Provers experienced elation, joy, increased confidence, enthusiasm and energy. On the other hand, there was lack of confidence, vulnerability, anxiety, decreased motivation, decreased concentration, lethargy, depression and indifference. There were sudden changes in mood and provers experienced marked irritability. On the physical level, many provers experienced headaches, irritation of the eyes, symptoms resembling allergic rhinitis, sore throats, nausea, heartburn, abdominal pain and flatulence, menstrual disturbances, lumbar pain, rheumatic joint pains, and skin eruptions. There were disturbances in normal sleep patterns, subjective perceptions of increased body temperature with hot flushes, and generalised tiredness and lethargy. Symptoms obtained from the proving of Hemachatus haemachatus were analysed as part of a comparative study with other remedies derived from snake venom: Lachesis muta, Naja tripudians, Elaps corallinus, Naja mossambica and Bitis arietans arietans. This comparison highlighted both the similarities and differences between these remedies and Hemachatus haemachatus.
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31

Mower, Gary W. "A comparative study on the effects of homoeopathically potentised Carbo vegetabilis on the growth rate of germinating Zea Mays seeds." Thesis, 2014. http://hdl.handle.net/10210/11545.

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M.Tech .(Homoeopathy)
The aim of this study was to evaluate the growth rate of germinating Zea Mays seeds subject to the administration of homoeopathically potentised Carbo vegetabilis in the potencies 12CH, 13CH and 14CH. The purpose of the study is to help disprove the popular "placebo effect" explanation as to why homoeopathy works by showing that homoeopathic medicine can have a fundamental effect on a living organism and thereby lend credibility to homoeopathy as a science. This study is of value as previous botanical studies have not attempted to provide an explanation as to how homoeopathic potencies may be acting and have mostly merely demonstrated their effects on cleoptile growth. Six hundred Zea Mays seeds were selected and planted in rolls of germination paper. There were 150 seeds in each of the three test groups as well as in the control group. The control group received distilled water only and the test groups their respective liquid potencies of Carbo vegetabilis, which were prepared using distilled water. The germination rolls were incubated at 24°C in darkness for a total of 135 hours. After 39 hours the germinating seeds were replanted into fresh germination rolls. The process was repeated at 87 hours after the first measurements were taken. The final measurements were taken at 135 hours. Shoot lengths and root lengths were recorded and overall lengths calculated. Mean shoot, root and overall lengths were expressed as percentages ofthe control using bar graphs. At 87 hours the potency that consistently decreased the growth of Zea Mays was the 13CH. The 12CH potency only decreased the shoot growth, whereas the 14CH improved root growth. At 135 hours overall growth was significantly decreased in all the test groups, but most markedly in the 12CH groups where root growth was drastically inhibited. When compared with the 87th hour measurement, the 13CH group showed a 13% increase in shoot growth. Carbo vegetabilis potencies 12CH, 13CH and 14CH were found to significantly influence the growth of germinating Zea Mays seeds.
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32

Pillay, Annette. "A comparative analysis of the Dream proving and Hahnemannian proving of an existing Homoeopathic remedy {Bitis arietans arietans}." Thesis, 2002. http://hdl.handle.net/10321/2771.

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Mini-dissertation submitted in partial compliance with the requirements for the Master's Degree in Technology: Homoeopathy, Homoeopathy at the Durban Institute of Technology, 2002.
Dream provings are considered to be a new era in Homoeopathy and as such are met with a lot of scepticism. They involve getting in touch with the dynamic influence of the remedy and observing this influence on the vital force in the form of symptoms (Dam, 1998: 128). Dreams are a main focus of the proving as they are considered to be the 'royal way to the psycho-dynamic depth of the state of the remedy being proved' (Dam, 1998: 128). The motivations for their acceptance or rejection are both reasonable. To determine if they are provings that should appear in the Materia Medica and Repertory it needed to be seen if they revealed the same features of a remedy that a classical proving provides.
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33

Macquet-Maurel, Louise. "The efficacy of Dioscorea villosa cream in the treatment of menopausal syndrome." Thesis, 2003. http://hdl.handle.net/10321/2774.

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Dissertation submitted in partial compliance with the requirements of the Masters Degree in Technology: Homoeopathy, Durban Institute of Technology, 2003.
The purpose of this randomised double-blind placebo-controlled study was to evaluate the efficacy of Oioscorea vil/osa cream in the treatment of menopausal syndrome in terms of subjective and objective data; and to compare the subjective data with that obtained from a concurrent study of ProgestoNat\xAE cream (McTeer, 2003).
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34

Chhiba, Ujaswee. "A group analysis evaluation of selected synthetic recreational drug isolate remedies in terms of known materia medica." Thesis, 2013. http://hdl.handle.net/10321/923.

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Dissertation submitted in partial compliance with the requirements for the Master’s Degree in Technology: Homoeopathy, Durban University of Technology, 2013.
The addition of a large number of new remedies to the homoeopathic materia medica has made it challenging to select the correct remedy for a patient. Locating individual remedies within groups makes it easier to understand, remember and apply the information from the remedies. The aim of this research study was to evaluate common themes and symptomatology of homoeopathic remedies belonging to the synthetic recreational drug isolate group, as represented in the known homoeopathic materia medica and repertory. Most remedies derived from synthetic recreational drug isolate sources have not been well documented or comprehensively proven in homoeopathy, so are not well represented in repertory programs. Therefore, in addition, remedies in this study were selected according to the homoeopathic significance of each remedy, the availability of actual provings and representation in materia medica, the existence of a synthetic derivative of the drug, and if the drug was commonly used. The selected remedies were then subjected to a manual rubric extraction process in which common rubrics were extracted. The common rubrics were analyzed to determine common sensations within the group. The extracted sensations were then defined using a dictionary and synonyms were determined using a thesaurus. Each sensation was subjected to a literature search to test its validity. Second and third order analyses were performed based on the results. The most common sensations found as a result of this process were: dryness, itching, fear, anger, restlessness, anxiety, indifference, heaviness, heat, acute and weakness. The active and passive reactions and compensations of the synthetic recreational drug isolate group were also analyzed. The active reactions included anger, rage, acute, violence, impatience and irritation. Passive reactions were heaviness, numbness, dullness, faintness, weakness and coldness. The compensatory reaction included sensations of ecstasy, elation and euphoria or tranquillity. Each remedy was classified into specific miasms based on Sankaran’s miasmatic model (Sankaran, 1997). Each remedy was categorized as a particular miasm if the literature showed a clear predominance of the themes associated with that miasm. Many of the remedies had features of the AIDS, Cancer, Sycotic and Tubercular miasms. Pathological tendencies of the synthetic recreational drug isolate group involved the throat, eyes, stomach, nervous system, male genitalia and sleep patterns. Clinically, the remedies can be used in cases of mental disorders such as psychosis and schizophrenia, chronic fatigue, visual and sleeping disorders, anorexia nervosa and neurological disorders such as chorea, tremors and formication. The results of this study appear to confirm the application of the group analysis methodology as outlined by Sankaran (2002). The results also add depth to the existing literature on synthetic recreational drug isolate remedies.
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35

Naidoo, Melanie. "A comparison of the results of a triple blind proving of Strychnos henningsii 30CH with the materia medica of existing remedies showing repertorial similarity." Thesis, 2010. http://hdl.handle.net/10321/547.

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Dissertation submitted in partial compliance with the requirements of the Master’s Degree in Technology: Homoeopathy, Durban University of Technology, 2010.
The purpose of this investigation was to determine the effect of Strychnos henningsii 30CH on healthy provers, and to compare these signs and symptoms to a selection of remedies sharing commonality with prominent rubrics. It was hypothesised that the 30CH potency of Strychnos henningsii would produce clearly observable signs and symptoms in healthy provers. It was further hypothesised that a comparison of Strychnos henningsii to those remedies yielding the highest numerical value and total number of rubrics on repertorisation of the proving symptoms would highlight differences and similarities between Strychnos henningsii and other existing homoeopathic remedies so that confusion as to its therapeutic indication is reduced. METHODOLOGY A mixed-method, triple-blind, placebo-controlled proving of Strychnos henningsii 30CH was conducted on thirty-two healthy volunteers who met specific inclusion criteria. Sixteen of the thirty-two provers received independently assigned placebo, with neither researcher nor prover knowing who was on placebo. A homoeopathic case history was taken and a thorough physical examination performed on provers before commencement of the proving. Data collection was in the form of a journal. On completion of the proving, the information from each journal was collated and assessed by the four researchers. The symptoms elicited were then translated into materia medica and repertory language, and a homoeopathic picture of the remedy emerged. Data from the case histories, physical examinations and group discussions were also considered. A repertorisation of 37 rubrics chosen to represent the essence of Strychnos henningsii was done using Radar 9.0. Exclusion repertorisation then followed, in order to identify those remedies producing the highest numerical value and total number of rubrics within the animal, mineral and plant kingdoms, and Loganiaceae family respectively. iii RESULTS A total number of 877 rubrics were produced. Exclusion repertorisation yielded the basis for comparison to the remedies from the animal kingdom namely Sepia which repertorised the highest, followed closely by Calcarea carbonica. Exclusion repertorisation of remedies from the mineral kingdom showed basis for comparison with Natrum carbonicum, Arsenicum album and Causticum, and from the plant kingdom, Lycopodium clavatum, China officinalis, Staphysagria and Rhus toxicodendron. Within the Loganiaceae family Nux vomica and Ignatia amara repertorised the highest, although Spigelia anthelmia, Gelsemium sempervirens and Strychninum also shared striking similarities with Strychnos henningsii. CONCLUSION The investigation clearly supported the hypothesis that Strychnos henningsii 30CH would produce observable signs and symptoms in healthy provers. The subsequent comparison of Strychnos henningsii proving symptoms to the materia medica of Sepia, Calcarea carbonica, Natrum carbonicum, Arsenicum album, Causticum, Lycopodium clavatum, China officinalis, Staphysagria, Rhus toxicodendron, Nux vomica, Ignatia amara, Spigelia anthelmia, Gelsemium sempervirens and Strychininum highlighted the similarities and differences between these remedies and Strychnos henningsii.
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36

Long, Bryan Henry. "A study of the relationship between the natural history of the Solanaceae species and the general and mental symptomatology of the Solanaceae remedies utilised in homoeopathy." Thesis, 2011. http://hdl.handle.net/10321/664.

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Dissertation submitted in partial compliance with the requirements for the Master‟s Degree in Technology: Homoeopathy, Durban University of Technology, 2011.
Until recently, various attempts have been made to simplify the prescription process in homoeopathic prescribing. The doctrine of signatures, miasmatic theory, the homoeopathic repertory and more recently, kingdom analysis by authors such as Sankaran (1994) and Scholten (1993) are some of the attempts that have been made to understand the materia medica. With the materia medica constantly expanding and considering that plants make up a significant percentage of the materia medica (Kayne, 2006), it is evident that new systems of homoeopathic prescribing are continually needed to help practitioners both study the remedies and prescribe more accurately. Aim The Solanaceae plant family are an important and well utilised plant family in homoeopathy (Vermeulen, 2004). Considering this, it was felt that a study investigating the relationship of the natural history of the family to its general and mental symptoms be conducted in order to apply a previously unexplored research paradigm in order to create a greater understanding of Solanaceae remedies utilised in homoeopathy. The study conducted was a non empirical correlation study of the Solanaceae plant family‟s natural history and general and mental symptoms manifested in Solanaceae remedies utilised in homoeopathy. The aims of the study were to establish if commonalties existed between general and mental symptoms of individual remedies belonging the Solanaceae family and their natural histories, as well as to establish if collective commonalities and correlations existed between the general and mental symptoms and the natural history of the Solanaceae family as a whole. Methodology The homoeopathic remedies obtained from the Solanaceae family of plants for the study were analysed in terms of rubric representation (size) using homoeopathic software packages, Radar 10.4 (Archibel, 2009b) and v Encyclopedia Homoeopathica (Archibel, 2009a) a sample selection was chosen. This selection was analysed in terms of general and mental rubrics. Qualitative thematic analysis was used to establish commonalities in keyword concepts between the respective natural histories of the studied family and their respective general and mental symptoms. Keywords obtained from data tables which included criteria such as habitat and distribution, plant description, active principles (primary alkaloids), uses, physiological action if ingested, historical significance, mythology and toxicology were subjected to thesaurus consultation and tabulated in an attempt to identify synonyms relating to the general and mental symptoms of individual remedies of the sample group in the study. This facilitated in the grouping of similar themes. Once commonalities pertaining to each individual species and remedy was further tabulated and discussed in terms of keywords relating to their natural histories, a collective analysis of common correlations between the plant family as a whole was performed. Results Common themes related to general and mental symptoms and to the natural histories of species in the study included “aggression” found in Atropa belladonna, “depression” found in Solanum dulcamara, “anxiety” found in Datura stramonium, “confusion” found in Hyoscyamus niger, “burns” found in Capsicum annuum, “ convulsions” found in Nicotiana tabacum , “ hallucinations” found in Mandragora officinarum and “delirium” found in Solanum nigrum. Common themes relating to general and mental symptoms and the natural history of the Solanaceae plant family as a whole included convulsions, hallucinations, confusion and anxiety. These themes were further compared to themes exhibited in Solanaceae studies conducted by Mangialavori (2007) and Sankaran (2002).
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37

Hoosen, Asima Goolam. "A homoeopathic drug proving of Acridotheres tristis." Thesis, 2010. http://hdl.handle.net/10321/695.

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Mini-dissertation submitted in partial compliance with the requirements for the Master's Degree in Technology: Homoeopathy, Durban University of Technology, 2010.
Introduction The aim of the study was to determine the effect of Acridotheres tristis 30CH on healthy volunteers (provers) and to record the clearly observable signs and symptoms produced, so that Acridotheres tristis 30CH may be prescribed according to the Law of Similars, as required by homoeopathy. Methodology The proving of Acridotheres tristis took the form of a randomised, placebocontrolled trial on 30 healthy volunteers who met inclusion criteria. The 30th centesimal potency of the tail feather was administered as lactose powders and fifty percent of provers were randomly administered an identical placebo-control substance. The collection of the data from the provers took the form of a journal in which each prover‟s symptoms were recorded for six weeks, including a one-week observation period prior to taking the powders, and a proving period of five weeks after administration of powders. On completion of the proving, each journal was assessed by the researcher to determine the suitability of the recorded symptoms for inclusion in the materia medica of Acridotheres tristis. These symptoms were then translated into the language of the materia medica and repertory and the remedy picture then formulated. Data from case histories, physical examinations and group discussions were also taken into account during the analysis of the proving symptoms. Results The homoeopathic drug proving of Acridotheres tristis, conducted as a doubleiii blind, randomised and placebo-controlled study produced a wide range of symptoms. In the collated edited data arising from the proving 396 journal entries were extracted and 595 rubrics in total were formulated, of which 56 rubrics were new. The main symptoms belonging to the mental and emotional spheres of this remedy include depression, anxiety, memory weakness and isolation accompanied by a need for solitude. The characteristic physical symptoms include headaches, dizziness, extreme fatigue, skin eruptions especially pimples and rashes, haemorrhoids, numbness and severe dysmenorrhoea. Other symptoms indicate a possible use in the treatment of gastro-intestinal complaints which include nausea, abdominal cramps, abdominal distention and heartburn. Conclusion The investigation supported the hypothesis that Acridotheres tristis would produce clearly observable signs and symptoms in healthy volunteers. It is essential that the proving symptoms be verified and expanded through clinical trials and further provings of Acridotheres tristis in various potencies, so that it becomes well-utilized remedy in the future.
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Peter, Clarissa. "A homoeopathic proving of the African lioness (Panthera leo) with a subsequent comparison with lion ethology." Thesis, 2015. http://hdl.handle.net/10321/1339.

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Submitted in partial compliance with the requirements of the Master’s Degree in Technology: Homoeopathy, Department of Homeopathy, Durban University of Technology, Durban, South Africa, 2015.
INTRODUCTION A homoeopathic drug proving was conducted by Master’s students at the Durban University of Technology (DUT). The proving substance was nail shavings obtained from an African lioness (Panthera leo). The primary objective of this study was to identify the symptoms produced by healthy individuals in response to Panthera leo 30CH; this was done by administering the proving remedy (Panthera leo 30CH) to healthy individuals, who recorded the symptoms they experienced after taking the remedy. The secondary objective was to compare the symptoms produced to the ethology of the African lion. The final objective was to further develop the materia medica by adding the remedy picture of Panthera leo. METHODOLOGY This study was qualitative and exploratory in nature. The study took the form of a randomised, double-blind and placebo controlled trial. A total of 30 provers, who met the inclusion criteria (Appendix C), participated in this study. The provers were randomly assigned to either a verum or placebo group, such that 24 received verum (Panthera leo) and 6 received placebo. Neither provers nor researchers had knowledge of which provers were in each group until the study was complete, and provers did not have any knowledge regarding the nature of the proving substance. Before commencing the study all provers signed relevant information and consent documents. The researcher then took a full case history and performed a physical examination. Provers recorded their baseline state for 7 days in a journal, prior to taking the verum or placebo, as administered to them. After recording their baseline state for 7 days, they took their remedies and continued to record their symptoms for a minimum of 2 weeks, or until the proving symptoms ceased. Once they had completed recording in their journals, a post-proving case history was taken and a physical examination was performed. All journals were collected and analysed by the researcher. The remedy was manufactured by triturating the crude substance up to the 3rd centesimal potency. This was then converted to a liquid potency and further diluted up to the 30th centesimal potency. Neutral granules were impregnated with Panthera leo 30CH, and dispensed as 10 granules in 500mg of lactose powder. The placebo was dispensed as 10 granules, which were impregnated with 96% ethanol, in 500mg lactose powder. Each prover received 6 lactose powders, containing either verum or placebo. The manufacture of Panthera leo was done according to the methods and guidelines stipulated in the German Homoeopathic Pharmacopoeia (Benyunes, 2005) RESULTS The proving of Panthera leo 30CH produced a total of 1234 rubrics, which represent a wide variety of mental, emotional and physical symptoms. The main themes that emerged from the mental and emotional symptoms included anger, aggression, irritability, poor concentration and fear. Physical symptoms included catarrh, constipation, diarrhoea, diminished appetite, fatigue, insomnia, thirstiness and headaches. A comparison was made between the symptomatology of Panthera leo and the ethology of the lion. Some of the themes of symptoms which corresponded with the ethology of the lion included ‘anger’, ‘audacity’, ‘ennui’, ‘increased appetite and thirst’, ‘responsibilities’ and ‘children’. CONCLUSION The objectives of this study were fulfilled, as the proving of Panthera leo produced a wide variety of clearly identifiable and observable symptoms amongst the healthy individuals recruited. There was a remarkable correlation of a portion of the materia medica with the ethological features of the African lion. As a result of this study, the materia medica of Panthera leo was well outlined and will be added to the existing body of homoeopathic materia medica for application and utilization in clinical practice
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39

Phahamane, Edward Peter. "A group analysis evaluation of the selected members of the acidum family of homoeopathic remedies in terms of known materia medica." Thesis, 2015. http://hdl.handle.net/10321/1338.

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Submitted in partial compliance with the requirements of the Master’s Degree in Technology: Homoeopathy, Department of Homeopathy, Durban University of Technology, Durban, South Africa, 2015.
Homoeopathy has advanced as an empirical art and has become a modern age science backed by the kind of massive research data and critical reviews that helps scientific knowledge become acceptable within the global knowledge space. Two centuries ago, the practice of homoeopathy was possible with a few hundred proven remedies of that time but as this science developed through both research and collection of empirical data the number of remedies available increased exponentially. As both the study of remedies and the remedy selection process became more challenging, group analysis by famous homoeopaths such as Farrington (1992), Sankaran (2003), Scholten (1993), Mangliavori (in Vidal 2005) emerged. Currently, with a database of over 3000 remedies available for prescription, group analysis, though a contested approach has proven to be an adequate tool that helps consolidate mass homoeopathic data into meaningful groupings that makes both the study of remedies and their application in practice easier. Classifying homoeopathic remedies into groups by means of group analysis and allowing such methods and results thereof to go through rigorous critiquing refines homoeopathic knowledge and improves its ability to sustain itself as a competent science. Homoeopathy has emerged as a technologically inclined science, utilising various software programs enabling more thorough correlation of symptoms and remedies and so improving the prescription process. Software programs have proven to be very useful tools for the development of group analysis. The aim of this study was to extract the common characteristic symptomatology of five selected homoeopathic remedies belonging to the acidum family as represented in the known materia medica and repertory. The acidum remedies appearing in Radar® 10 repertory (Archibel 2008) were analysed in terms of rubric representation (frequency) and the top five were selected for inclusion in the study. The top five remedies were: Nitricum acidum, Phosphoricum acidum, Muriatic acidum, Sulphuricum acidum and Fluoricum acidum. All rubrics in which the selected remedies appeared were extracted using the homoeopathic software package Radar® 10 (Archibel, 2008) and analysed for sensations and active, passive and compensation reactions of the selected remedies, as per Sankaran (2002). The common primary sensations identified were, burning, sore, swelling, pressing, cramping, dryness, weakness, tearing, and coldness. There were also sensations of anxiety, restlessness, delirium, delusions, dullness, sadness and cheerfulness. Active reactions identified were: hot, heat, inflammation and sensitivity. Passive reactions identified were: coldness, numbness and weakness. Compensation reactions identified were: restlessness, hurriedness, intense reaction and passion. Miasmatic keywords as per Sankaran (2002) were used to determine the miasmatic tendencies of the selected top five acidum remedies. In general all acidum remedies appeared to have a dominant syphilitic miasmatic tendency but acidums were present through all the miasms. Their miasmatic tendencies are easily recognised when viewed in the light of their pathophysiological processes. The pathological tendencies of acidum remedies examined in this study include: haemorrhoids, general haemorrhage, syphilis, warts, neoplastic and non-plastic tumours, irritable bowel syndrome (reflux, colic, constipation), rheumatism, muco-cutaneous ulcerations (STIs, Xerostomia, diabetic ulcers) and bone diseases (osteoporosis, osteitis, and peri-osteitis). The results of this research were compared to the findings of Scholten (1993) and Mangialavori and Marotta (2005). It is the researcher’s view that Sankaran’s methodology of group analysis which he used to explore biological groups of remedies (plants and animals) is adequate for use with non-biological groups of remedies such as mineral acidums. The researcher found group analysis methodology worthy as a tool for classifying the mass data of acidum remedies into orderly sets of meaningful data. Group analysis is consistent with the laws and principles of homoeopathy and encourages the use of materia medica and repertory which are fundamental to the study and application of homoeopathic knowledge.
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40

Ive, Elaine Catherine. "An in-vitro assessment of the effects of Arsenicum album (30CH and 200CH) on leukocytes previously antagonised by arsenic trioxide." Thesis, 2010. http://hdl.handle.net/10321/590.

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Dissertation submitted in partial compliance with the requirements of the Master's Degree in Technology: Homoeopathy, Durban University of Technology, 2010.
The therapeutic effects of homoeopathic Arsenicum album potencies were investigated in-vitro, using human cell cultures which were previously antagonised by arsenic trioxide (As2O3). Primary cell culture (peripheral blood mononuclear cells) and a continuous cell line (MT4) were treated with succussed and unsuccussed homoeopathic potencies, 6CH, 30CH and 200CH. This study aimed to verify the homoeopathic law of similars and to determine whether potencies diluted beyond Avogadro’s constant had physiological effects on cells; whether various potencies would cause different effects as proposed by the Arndt-Schultz law; whether succussed and unsuccussed homoeopathic potencies had different effects on the cells; and to establish whether a biotechnological method could be used to evaluate the above. Initial experiments involved isolation and culturing of the peripheral blood mononuclear cells (PBMCs) and the MT4 cell line. Cell titres were determined using the trypan blue dye exclusion assay. The solubilization method of As2O3 was optimized through various dissolution experiments, so as to attain a homogenous arsenical solution. The MTT assay was used to measure the percentage cytotoxicity and the half maximal inhibitory concentration (IC50) caused by the antagonist As2O3 on the PBMCs and the MT4 cell line. The two cell cultures were compared with regard to their susceptibility to As2O3 and their reliability of response. The homoeopathic potencies of Arsenicum album (6CH, 30CH and 200CH) were prepared by initially triturating the As2O3, and then either hand succussing 10 times (succussed) or allowing to diffuse for 30 s (unsuccussed) in sterile distilled water, with the final potencies made up in cell culture media, RPMI. The MTT assay was used to determine the percentage cell viability when the As2O3-antagonised cells were treated with the Arsenicum album potencies. All assays were performed in triplicate. v The As2O3 was found to fully dissolve when 396 mg of dry As2O3 was added to 100 mL of sterile distilled Milli-Q water, which was left to stand for 10 days at 80°C. The cytotoxicity results showed that the PBMCs were not as reliable as the MT4 cells, which showed significant susceptibility to the As2O3. The IC50 of As2O3 on 1 mL of MT4 cells was found to be 5 μM As2O3 (133 μL) for 48 h. The trypan blue dye exclusion assay demonstrated that the viable MT4 cells decreased in number after exposure to the As2O3, with an increase in number of the non-viable cells. Microscopically, the cells were fewer in number and displayed signs of possible blebbing and cell shrinkage, showing potential cell death due to apoptosis. The cell viability results showed that the Arsenicum album 6CH resulted in the lowest absorbance readings and the Arsenicum album 200CH gave the highest readings; this verified the therapeutic effects of homoeopathic remedies when given according to the law of similars; that potencies diluted beyond Avogadro’s constant had stimulating effects; and that the more dilute potencies stimulated recovery in the cells more than the lower potencies, verifying the Arndt-Schultz law. The treatments and the times of exposure were found to be statistically significant determinants of cell viability, whereas succussion did not cause any significant variation in the results. The study thereby provided evidence that a biotechnological method could be used to scientifically evaluate the physiological effects of homoeopathic potencies on human cells; that the homoeopathic potencies did have therapeutic effects; and that succussion was not required in the potentization method in order to produce a curative remedy.
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41

Maharaj, Poonam. "A comparison between the traditional use of Strychnos henningsii and the homoeopathic indications of Strychnos henningsii 30CH." Thesis, 2010. http://hdl.handle.net/10321/594.

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Mini-dissertation submitted in partial compliance with the requirements for the Master’s Degree in Technology: Homoeopathy, Durban University of Technology, 2010.
The purpose of this study was to investigate the homoeopathic indications of the bark of the Strychnos henningsii tree, through a homoeopathic proving, and to subsequently compare these results to the documented traditional use of the crude substance. Methodology The study design took the form of a triple-blind placebo-controlled trial consisting of 32 participants who met defined inclusion criterion. These participants were randomly divided into four groups, each consisting of eight provers and supervised by one of four M. Tech Homoeopathy students. Fifty percent received placebo and fifty percent received verum. Neither the researcher nor the provers were aware of the nature of the proving substance as well as who received the placebo and who received the verum until the study was completed. The proving substance was administered in the 30CH potency, according to an ECH (European Committee of Homoeopathy) methodology. All provers were subjected to pre – and post -proving consultations in which case histories and physical examinations were performed. A pre-proving workshop was held for all provers and supervisors. Symptom collection was done by using information obtained from prover journals which was then collated, edited and translated into repertory language. By identifying broad areas of traditional use of Strychnos henningsii and relating these to rubrics derived from the proving of Strychnos henningsii 30 CH, a comparison was performed in order to evaluate the overlap between the homoeopathic indications and traditional use of the proving substance. Results After critical evaluation, it was found that whilst overlaps exist in the treatment of liver disease, nausea, dysmenorrhea, rheumatism, chest pain, malaria and dizziness, no overlap was found in the use of the homoeopathic remedy in snakebites. In addition the proving revealed symptoms that were not indicated in traditional use such as headaches, asthma, influenza, sinusitis and hayfever, as well as infections of the eye, ear, nose and throat. Conclusion Thus, upon comparison of the traditional uses of Strychnos henningsii to the symptoms produced in the proving of Strychnos henningsii 30CH, revealed that similarities pertaining mainly to the gastro-intestinal system, female gynaecological tract and rheumatic complaints exist. However, the proving elicited many new symptoms that are purely homoeopathic, these included head, mind, sleep, dream, nose, ear, chest and respiratory symptoms. Furthermore, it is hoped that further provings of this substance at different potencies would contribute further to the materia medica of the substance.
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42

Gryn, Agnieszka. "A comparison of the results from the proving of Erythrina lysistemon 30CH, with toxicology of the crude substance." Thesis, 2007. http://hdl.handle.net/10321/401.

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Mini-dissertation submitted in partial compliance with the requirements of the Master's Degree in Technology: Homoeopathy in the Faculty of Health Sciences at the Durban University of Technology, 2007
The homoeopathic drug proving of Erythrina lysistemon 30CH took a form of a randomised triple–blind, placebo–controlled study. This trial was conducted at the Homoeopathic Day Clinic on the premises of Durban University of Technology. The research group consisted of 32 provers, which were recruited from amongst practicing homoeopaths, homoeopathic students (2`nd–5`th year), as well as patients of the Homoeopathic Day Clinic (DUT) and their relatives. The participation was purely on voluntary basis. Provers were randomly divided into two groups: a placebo group of 12; a proving group of 20. Each researcher supervised 8 provers. Neither the provers, nor the researchers were aware of the name or nature of the substance being proved, and whether a prover is receiving a placebo or the proving substance until the unblinding process. Provers had a homoeopathic case history taken and a physical examination performed on them before commencement of the proving to establish each individual’s baseline. Provers were required to keep journals in which they recorded their sign and symptoms: starting 7 days prior to commencing the proving, throughout the proving, as well as after administration of the remedy formulated. All the information gathered was then correlated and interpreted by the researchers i.e. four M.Tech.Hom students. Subsequent translation of the symptoms into materia medica and repertory language took place. On completion of the proving a homoeopathic picture of the remedy with III distinct affinities was established. Those affinities were then compared to the toxicology of the major chemical constituents of Erythrina lysistemon. Data was then analyzed by qualitative methods for it was not amendable to standard statistical analysis.
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43

Lockhat, Irfana. "A comparison of the results of a triple-blind homoeopathic drug proving of Strychnos henningsii 30CH with the toxicology of the crude substance." Thesis, 2010. http://hdl.handle.net/10321/600.

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Dissertation submitted in partial compliance with the requirements of the Master’s Degree in Technology: Homoeopathy, Durban University of Technology, 2010.
The homoeopathic drug proving of Strychnos henningsii 30CH took the form of a mixed-method triple-blind, placebo-controlled study. The purpose of the study was to compare the results of the triple-blind homoeopathic drug proving with the toxicology of the crude substance. Methodology Thirty-two provers were selected and randomly divided into four equal groups of 8 provers, with each group supervised by one of four M.Tech.Hom student researchers. Fifty percent of the subjects (16 or the 32) received placebo in a random manner. Provers recorded their state in journals for one week prior to commencing the verum/ placebo powders. Data was extracted from journals and combined with case histories, physical examinations to compile the proving profile. The data derived from journals and case histories were edited and collated and thereafter reformatted and classified according to standard materia medica and repertory conventions. This constituted the homoeopathic remedy picture which was then compared to the toxicity of the major chemical constituents of Strychnos henningsii by qualitative methods. Results Provers produced symptoms on the mental, physical and emotional levels. There was a distinct similarity between the toxicology of Strychnos henningsii in its iii crude form, and a majority of the symptomatology obtained during the proving. The comparison of Strychnos henningsii proving symptoms and that of the crude substance was demonstrated by the proving symptoms showing similarity with the chemical constituents of the bark. The bark contained alkaloids which demonstrated similar symptoms in poisonings as described by the provers. The alkaloids found in the Strychnos henningsii bark were strychnine, diaboline, holstiine, strychnochromine and guianensine. Conclusions This homeopathic proving of Strychnos henningsii allowed for successful comparison between the alkaloids contained in the bark and the proving symptomatology. Notwithstanding the successful comparison and noted levels of overlap, it was observed that prior knowledge of homeopathy was beneficial to the provers. Furthermore, the researcher argues that the triple blind method employed is effective, but may hinder the researcher during analysis and that it is important that toxicological information about any substance should be obtained before a proving commences.
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44

Somaru, Nevorndutt. "An investigation of the concept of homoeopathic imponderabilia using a Hahnemannian proving of focused pink light." Thesis, 2008. http://hdl.handle.net/10321/340.

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Thesis (M.Tech.: Homoeopathy)- Dept. of Homoeopathy, Durban University of Technology, 2008. xvi, 256 leaves.
Conduct a randomised, double blind, placebo controlled study in order to determine the sphere of action of the imponderable remedy Pink 30CH on healthy volunteers who recorded the signs and symptoms produced in order to determine the substances potential usefulness in a future clinical setting according to the Law of Similars. Determine and highlight the commonalities shared between the symptoms and themes produced by remedy Pink 30CH and the other selected imponderable remedies. In the homoeopathic drug proving of remedy Pink 30CH, provers were uninformed to both the nature of the substance as well as to the potency selected and used for proving purposes. Neither the provers nor the research investigator had any knowledge of who received the verum or the placebo until the end of the proving. Thirty (30) provers were selected after meeting the inclusion criteria of which thirty percent (30%) of the subjects received placebo in a randomised fashion. Verum and placebo were dispensed to the proving body in a set of six (6) powders which were taken sublingually three (3) times daily or until any proving symptoms were experienced. All provers were examined and made to record in their journals before, during and after the administration of the proving substance so as to serve as their own intra-individual controls. At the end of the proving period all journals were then recalled and all proving data recorded was then collated and edited into a repertory and materia medica format, which was then used to formulate a homoeopathic drug picture of the remedy that could be used in future clinical settings. The homoeopathic drug picture thus derived was then analysed with the aim of highlighting the important themes that were elicited during the proving. These symptoms and themes were then related and compared to seven (7) other imponderable remedies: Luna (Moonlight); Magnetis Polus Arcticus (North pole of the magnet); Magnetis Polus Australis (South pole of the magnet); Positronium (Anti-matter); Radium bromatum (Radium bromide); Sol (Sunlight) and X-ray, in order to expand the overall understanding of the commonalities shared by the imponderabilia as an entirety.
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45

Hull, Ruth Heather. "A group analysis evaluation of the selected psychoactive plant remedies in terms of known materia medica." Thesis, 2016. http://hdl.handle.net/10321/1771.

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Submitted in partial compliance with the requirements of the Master’s Degree in Technology: Homoeopathy, Durban University of Technology, Durban, South Africa, 2016.
There are now several thousand remedies available to a homoeopath and this number is continually increasing with the increase in homoeopathic research and provings. This growing wealth of data does, however, make choosing a homoeopathic remedy difficult and some homoeopaths argue that the essence of homoeopathic remedies are being lost in this excess of data. In an attempt to more accurately see a remedy’s ‘picture’ and gain deeper insight into remedies, Scholten (1993), Sankaran (2005a) and Mangialavori (2010) developed different methods which can now be collectively referred to as “group analysis”. The aim of group analysis is to find symptoms, sensations and pathological tendencies that are common to all remedies within a group. This study involved applying Sankaran’s group analysis approach to the psychoactive plant drug remedies with the rationale of filtering and organizing the mass of data we now have available on this group. This will enable both students and professionals of homoeopathy to develop a deeper understanding, and hence greater utilization, of the psychoactive plant drug remedies. The following five homoeopathic remedies were chosen for this study on the grounds that they have all been extensively proved through both homoeopathic provings and cured clinical cases and there is a vast amount of literature available on these remedies in materia medica and repertories: • Anhalonium lewinii (Cactaceae family) • Cannabis indica (Hamamalidae family) • Coffea cruda (Rubiaceae family) • Nux moschata (Magnolianae family) • Opium (Papaveraceae family) A computer repertory search was conducted using RadarOpus (Archibel, 2014) to extract all rubrics containing the selected remedies. Parameters were set to retain only rubrics that have less than 50 remedies and at least two of the selected psychoactive plant remedies in them. This was to ensure that only well-defined, characteristic remedies were looked at. The rubrics were visually analyzed, compared and contrasted to determine the common sensations within them and mental, general and particular symptoms were analyzed in terms of Sankaran’s model of Vital Sensation (2005a). The vital sensation of the psychoactive plant drug remedies was found to be that of horror, fear or fright. All the remedies belonging to this group experience the sensation of horror either through their perception of pain or through dreams, visions, hallucinations or anxiety. This sensation pervades all these remedies which are constantly trying to escape this sensation by either increasing or decreasing their activity and sensitivity. The active reaction to the sensation of horror is to increase activity. This is expressed through increased sensitivity; mental clarity; sensations of contraction, fullness, heaviness, heat or moisture; delirium, hallucinations and instability. The passive reaction to the sensation of horror is to decrease activity. This is expressed through insensitivity; lack of mental clarity; sensations of expansion, emptiness, lightness, cold or dryness; sleep, stupor and unconsciousness. The compensation, or coping mechanism that psychoactive plant drug remedies develop, is a transcendence of their condition: they transcend, or escape, their condition by no longer feeling or doing anything, by becoming numb and insensitive. The researcher suggests that although the remedies of the psychoactive plant drug group can be classified according to different miasms, the over-riding miasm of this group is the sycotic miasm with its fundamental sense of having a ‘fixed weakness’ within themselves. The researcher also proposes that the psychoactive plant remedies have an affinity for the central nervous system and for ailments caused by strong emotions such as joy, anger, excitement, fear or fright. These remedies tend to produce pathologies of the central nervous system and sleep including increased reflexes, involuntary motions, trembling, jerking; weakness, atrophy, slowness, paralysis; unconsciousness; catalepsy; Autism Spectrum Disorders; hypersensitivity; insensitivity or absence of sensitivity; pain; formication; mental confusion, poor comprehension, nonsensical speech; memory disorders; delirium, hallucinations, schizophrenia; mood disorders; behavioural disorders; anxiety; insomnia, narcolepsy and nightmares. The researcher found group analysis to be a powerful methodology that, if employed correctly, can aid homoeopaths to learn and understand remedies in their ‘totality’.
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46

Naidoo, Nalini. "A homoeopathic drug proving of Carcharhinus leucas 30CH and a subsequent comparison with that of Galeocerdo cuvier hepar 30CH." Thesis, 2018. http://hdl.handle.net/10321/3083.

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Submitted in partial compliance with the requirements of the Master’s Degree in Technology: Homoeopathy, Durban University of Technology, Durban, South Africa, 2018.
Introduction The aim of this study was to conduct a homoeopathic proving of Carcharhinus leucas in the thirtieth centesimal potency (30CH) and to subsequently establish and describe the symptomatology in standard materia medica format and then compare this symptomatology to Galeocerdo cuvier hepar 30CH. Methodology The homoeopathic proving of Carcharhinus leucas 30CH was conducted at the Durban University of Technology and was accomplished by means of a randomised, double blind, placebo controlled trial. Carcharhinus leucas 30CH was manufactured by the researchers according to Method 6, Method 8a and 10 of the German Homoeopathic Pharmacopoeia (Benyunes, 2005: 36-39). The homoeopathic proving was conducted in the form of a double blind placebo controlled study of Carcharhinus leucas 30CH with a total of 30 healthy provers. The prover sample was divided into two groups by a process of randomisation. Twenty four provers (80%) comprised the verum group and the remaining 6 provers (20%) comprised the placebo group. The identity of the proving substance and the potency used was not disclosed to provers. Provers documented their physical, mental and emotional status for one week preceding the administration of the proving remedy. A comprehensive physical examination and case history of every prover was taken before and after the proving period. Provers were instructed to ingest one powder three times a day for two days but were told to discontinue the powders once symptoms arose. The duration of the proving spanned 6 weeks and throughout the proving process, researchers were in constant communication with all the participants. Upon completion of the proving process, journals were collected and the information therein was translated into materia medica and repertory format. This was done in order to acquire the remedy picture of Carcharhinus leucas 30CH. Thereafter, the symptomatology of Carcharhinus leucas 30CH was compared to the symptomatology of Galeocerdo cuvier hepar 30CH. Results The proving of Carcharhinus leucas 30CH produced a total of 590 already existing rubrics and 43 new rubrics. The majority of these rubrics were located in the MIND (127), GENERALS (64), HEAD (55), EXTREMITIES (50), and EYE (34). In regard to the mind, prominent features were apparent such as anger, anxiety, cheerfulness, an aversion or amelioration within company, difficulty concentrating or increased focus, varying delusions and fears and irritability. Pertaining to the head, headaches were evident with varying concomitants and modalities, with headaches predominantly affecting the forehead and sides. Sensations included dryness, heat, heaviness, perspiration and shaking. The extremities displayed symptoms primarily in the forearms, legs and thighs and sensations included paralysis, shaking, swelling and weakness. In regard to the eye, eye pain with multiple modalities were apparent, with symptoms related to the canthi and eyelids. Sensations included heat, heaviness, inflammation, itching and photophobia as well as a visible discolouration of the eye. Analysis of the results presented an understanding of the similarities and differences between Carcharhinus leucas 30CH and Galeocerdo cuvier hepar 30CH. Conclusion As hypothesised, it was evident that administering Carcharhinus leucas 30CH to healthy individuals did yield observable symptomatology. Additionally, it was apparent that various correlations between Carcharhinus leucas 30CH and Galeocerdo cuvier hepar 30CH existed
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Leisegang, Kristian. "A group analysis evaluation of the kingdom fungi of homoeopathic remedies in terms of known materia medica." Thesis, 2007. http://hdl.handle.net/10321/34.

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Thesis (M.Tech.: Homoeopathy)-Dept. of Homoeopathy, Durban University of Technology, 2007 x, 95, [4] leaves, Annexures A-C
Until recently the most important method of studying homoeopathic remedies has been to look at each remedy separately and not in the context of a particular group to which it belongs. Group analysis, as defined by pioneering authors such as Sankaran (2002) and Scholten (1993), is an attempt to identify a mechanism for understanding groups of related remedies according to natural classification of the various sources used in homoeopathic practice.
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Botha, Izel. "Towards an integrated methodology : C4, Sherr and Dream provings of Protea cynaroides." Thesis, 2010. http://hdl.handle.net/10321/588.

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Submitted in fulfilment for the requirements of the Degree in Doctor of Technology: Homoeopathy, Durban University of Technology, 2010.
Homoeopathic provings form the experimental base of clinical homoeopathy. Provings are conducted through the administration of homoeopathically prepared medicine to healthy volunteers in order to elicit disease symptoms. The symptoms are collated to formulate the materia medica of the substance. AIM The aim of this study was to compare the most commonly employed proving methodologies, the C4 trituration, the Sherr and the Dream proving methodology, by application in order to ascertain the validity of the claims made in terms of the efficiency of the method to elicit reproducible symptoms. This study sought to follow the existing methodologies exactly as set out by the original developers with the aim of developing an integrated methodology. The order in which the three groups were assigned followed a logical sequence that ensured that the maximum efficiency would be obtained, and that the blinding process would not be compromised. The claims were investigated based on the hypotheses proving symptoms are reproducible when applying identical proving methodologies in consecutive years, that different methodologies yield different numbers, types and quality symptoms, that differences exist between the symptoms yielded by the placebo and the verum groups within the same methodology, and that an integrated methodology could be developed based on the study of the relative efficiency of the respective methodologies. METHOD During the course of the research, 70 provers were recruited to test the unknown substance through application of the three methodologies Page iii mentioned above. Each of the three groups comprised of 10 verum provers per year, thus totalling 20 verum provers per group. The second group had an additional 10 provers, comprised of five placebo provers for 2008 and 2009 respectively. RESULTS The rubrics produced in each group were statistically analysed. The results reflected a reasonable level of reproducibility, proving the first hypothesis, but highlighted the fact that different provers would result in different symptoms due to their individual susceptibility and sensitivity to the proving substance. This effectively proved the hypothesis that the proving effect was reproducible in consecutive years through the application of the same methodology. The result of the data collection was the formulation of 1 373 rubrics utilised for analysis purposes, resulting in 881 verified rubrics, that comprise the repertory for Protea cynaroides. From the data, it was evident that the C4 trituration and the Sherr proving methodologies yield the most rubrics. Not only do they yield a large number of rubrics, but they also yield a much larger number of rubrics than produced by the placebo portion of the Sherr proving methodology. In the Dream proving methodology group there is much less rubrics present at each rubric level than yielded by the C4 trituration and the Sherr proving methodologies. Strong chapter affinities were observable when applying the C4 and Sherr proving methodologies. The C4 methodology seem to favour the chapters dealing with the senses, evident in the Ear, Eye, Hearing, Mouth, Nose, Skin and Vision chapters where the C4 rubrics were more prevalent than the Sherr rubrics. The Sherr methodology was evident in the remainder of the chapters, indicating the wide applicability of this methodology. This proved the hypothesis that some proving methodologies are more effective than others. Page | iv The hypothesis of difference between the placebo and verum groups within the Sherr proving methodology was proven as it was evident in the number of rubrics produced by each section. The verum portion elicited 63 percent of the total rubrics compared to the placebo portion which only elicited 28 percent. Placebo provers thus elicit fewer symptoms during the proving process than verum provers, demonstrating that homoeopathic drug provings are not a placebo response, but that the administration of the medicine results in the development of clearly observable symptoms in the participants. As originally assumed, the proving did produce clearly observable symptoms in healthy provers. The symptoms gathered through the application of the methodologies were also comprehensive enough to develop a complete materia medica and repertory for Protea cynaroides. CONCLUSION From the data presented in the study, one can thus conclude that in order to elicit symptoms representing all 38 chapters present in the Protea cynaroides proving, the C4 trituration proving and the Sherr proving methodologies would have to be combined. Although Group two is able to elicit the majority of symptoms, it would be even more effective when it is combined with the C4 proving methodology, hence leading to the development of an integrated methodology combining these methods, proving the final hypothesis. The suggested integrated methodology thus comprises of firstly conducting a C4 trituration proving using at least 10 predominantly experienced C4 provers. This proving would serve to highlight the major themes. These themes can then be confirmed through secondly conducting a proving according to the Sherr methodology, in a group comprising of at least 17 provers, including a 10 percent placebo in the group. Repeated oral doses would be administered to the participants in this. At the conclusion of the second Page | v proving stage, all the data would be collated and formatted into a materia medica and repertory. It would, however, be important to prove the integrated methodology‘s usefulness through practical application, leading to the recommendation that the methodology be tested.
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49

Zondi, Gugulethu Moonlight. "A homoeopathic drug proving of Acacia Xanthophloea 30CH, with subsequent comparison to the doctrine of signatures." Thesis, 2016. http://hdl.handle.net/10321/2484.

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The objective of the following study was threefold: to conduct a homoeopathic drug proving of Acacia xanthophloea 30CH on healthy individuals in order to elucidate the totality of signs and symptoms produced by the drug substance; to analyse the signs and symptoms gathered from the proving, collate the data, and convert the symptoms into materia medica symptoms and rubrics; to compare the symptoms of the proving to the doctrine of signatures. Methodology This proving study was a double-blinded, placebo controlled study. Thirty provers or participants were recruited for the study and the sample size was divided equally between two researchers (A. Gobind and G. Zondi). The sample was randomly divided into two groups, with one group receiving an active substance (verum group) and the other group receiving a placebo (control group). Amongst the 30 provers, 24 participants received verum and six received placebo. Each prover was given a journal to record their symptoms, a pen and nine powders. The duration of this proving study was six weeks including the first week of baseline during which time each prover was required to record their symptoms before taking the proving substance. This procedure was clearly explained to each prover and an information sheet with detail explanation of the proving procedure was provided and informed consent obtained. A thorough case history was taken in the initial consultation and physical examinations to ensure that individuals participating met the inclusion criteria and were healthy. Results Information derived both researchers was combined and the extraction of signs and symptoms then commenced. The symptoms were translated into materia medica and repertory format and graded accordingly. Thereafter the symptoms that emerged from the study were discussed and compared with the doctrine of signatures of Acacia xanthophloea. Provers experienced a wide range of symptoms mentally and emotionally e.g. anger, poor concentration and focus, disconnected feeling, depression, stress, anxiety, antisocial/ aversion to company, tranquillity. A large number of physical symptoms were noted by provers e. g. headaches, ailments of extremities (joint pain, weakness), female related symptoms (irregular menses, decrease/ increase libido etc.), eye symptoms, skin symptoms and general symptoms. The comparison of the symptoms of Acacia xanthophloea 30CH to the doctrine of signatures of the tree Acacia xanthophloea illustrated certain similarities, especially with regard to skin symptoms, eye symptoms, gastrointestinal symptoms and headaches. Conclusion The proving substance Acacia xanthophloea 30CH did produced signs and symptoms when given to healthy individuals as hypothesised. The symptoms when compared to the doctrine of signatures of the acacia xanthophloea tree did show correlation as hypothesised.
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50

Naidoo, Kerusha. "A homoeopathic drug proving of Panthera leo with a subsequent comparison of Lac leoninum." Thesis, 2015. http://hdl.handle.net/10321/1335.

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Submitted in partial compliance with the requirements of the Master’s Degree in Technology: Homoeopathy, Department of Homepathy, Durban University of Technology, Durban, South Africa, 2015.
Introduction This study was a double-blind, placebo controlled proving of Panthera leo 30CH (claw of a African lioness); the aim being to determine the effect of this substance induces on healthy persons and in doing do explore the homoeopathic therapeutic potential thereof, in addition a subsequent comparison with the provings of Lac leoninum (milk of a lioness) (Sankaran,1998) (Herrick,1998) was performed. Objectives The primary objective of this proving was to determine the effect that Panthera leo 30 CH on healthy provers so that the therapeutic potential of the substance could be determined. The secondary objective was to compare the Materia medica of Panthera leo with that of Lac leoninum (Herrick, 1998) and Sankaran (1998). Lastly, the third objective was to further develop the homoeopathic Materia medica by adding the remedy picture of Panthera leo. Methodology The drug proving of Panthera leo was conducted as a randomized, exploratory, double blind placebo controlled study. Thirty participants (healthy volunteers) who met the inclusion criteria (Appendix B) participated in the proving, twenty – four were given the verum and the remaining six placebo. Upon obtaining written informed consent the researcher performed a full case history and comprehensive physical examination on each prover before commencement of the proving. A subsequent follow up case history and physical examination at the end of the proving was also performed to establish whether provers had returned to their respective healthy states. The provers took their first dose of the proving remedy at a dosage of 1 dose three times daily for 2 days and recorded all symptoms they experienced in their respective journals according to the guidelines in Appendix C. On completion of the proving, all provers handed in their journals which were then transcribed, assessed and analyzed. An extensive comparison between the proving of Panthera leo and the two provings of Lac leoninum (Herrick, 1998) (Sankaran, 1998) followed. The respective remedies were compared and contrasted with respect to Materia medica and repertory and similarities and differences highlighted. Results A total of 1255 rubrics were obtained of which the mind section of the Materia medica weighed heavily comprising 35 % (435 rubrics) of the proving symptoms, the generals section (11% = 135 rubrics) and head section (9% = 109 rubrics) respectively. Therefore it can be suggested that this remedy’s sphere of action is limited largely to the mind (emotional state) however unique physical indications specifically regarding headaches are also within its sphere of action. Of the total, 1255 rubrics that were obtained only 11% (138 rubrics) where shared with the two other provings of the African lion (Herrick 1998 & Sankaran 1998); as suggested by Naude (2011) one can speculate that these shared symptoms may represent the unique mammalian component of the animal the differences however considerably outweigh the similarities between these provings and for this reason one can conclude that factors in addition to the species of animal from which the remedy is sourced further influence the resultant proving symptoms. Conclusion It can be concluded that Panthera leo 30CH produced clearly observable symptoms in healthy provers who participated in this proving, furthermore there was clear congruency between certain aspects of this proving and that of Herrick and Sankaran however such similarities were limited.
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