Academic literature on the topic 'Homeopathic materia medica'
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Journal articles on the topic "Homeopathic materia medica"
Wood, Petra. "Homeopathic Cancer Drugs: Oncology Materia Medica." Homœopathic Links 31, no. 02 (June 2018): 168. http://dx.doi.org/10.1055/s-0038-1654692.
Full textWittenburg, Christine, and Jean Ellen Duckworth. "Comparison of aluminum toxicology and homeopathic Alumina: a mixed methods study." International Journal of High Dilution Research - ISSN 1982-6206 17, no. 1 (July 22, 2021): 08–09. http://dx.doi.org/10.51910/ijhdr.v17i1.897.
Full textTeixeira, Marcus Zulian. "Brief Homeopathic Pathogenetic Experimentation: A Unique Educational Tool in Brazil." Evidence-Based Complementary and Alternative Medicine 6, no. 3 (2009): 407–14. http://dx.doi.org/10.1093/ecam/nem128.
Full textBlock, Janice. "Nineteenth-Century Homeopathic Materia Medica Texts Predict Source Materials Whose Physiological Actions Influence Thyroid Activity." Homeopathy 108, no. 03 (March 14, 2019): 214–22. http://dx.doi.org/10.1055/s-0039-1677704.
Full textLees, P., L. Pelligand, M. Whiting, D. Chambers, P.-L. Toutain, and M. L. Whitehead. "Comparison of veterinary drugs and veterinary homeopathy: part 1." Veterinary Record 181, no. 7 (August 11, 2017): 170–76. http://dx.doi.org/10.1136/vr.104278.
Full textBricarello, Patrizia, and Edaciano Leandro Lösch. "Homeopathic repertorization in vegetables: a case study for the bell pepper culture (Capsicum annuum L, Solanaceae)." International Journal of High Dilution Research - ISSN 1982-6206 20, no. 2-3 (June 2, 2021): 24–33. http://dx.doi.org/10.51910/ijhdr.v20i2-3.1089.
Full textRuiz, G., J.-L. Torres, O. Michel, and R. Navarro. "Homeopathic effect on heart rate variability." British Homeopathic Journal 88, no. 03 (July 1999): 106–11. http://dx.doi.org/10.1054/homp.1999.0294.
Full textKara, Shamini, and Gyandas Wadhwani. "Two Clinical Experiences with a New Sarcode: Potentised Mitral Valve in LM Potencies." Homœopathic Links 31, no. 04 (December 2018): 241–47. http://dx.doi.org/10.1055/s-0038-1677545.
Full textPaul, John. "Differential Analysis of Homeopathic Medicines Attributed to Pride." Homœopathic Links 31, no. 03 (September 2018): 184–86. http://dx.doi.org/10.1055/s-0038-1669958.
Full textGypser, Klaus-Henning. "The Necessity and Procedure of the Revision of the Homeopathic Materia Medica." Homoeopathic Links 25, no. 01 (March 2012): 9–12. http://dx.doi.org/10.1055/s-0031-1298195.
Full textDissertations / Theses on the topic "Homeopathic materia medica"
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.
Full textGoote, 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.
Full textC4 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.
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.
Full textThe 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.
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.
Full textBackground : 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.
Full textAim: 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.
Full textIntroduction 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.
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.
Full textIt 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.
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.
Full textBackground 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.
Full textDysmenorrhoea 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.
Full textProvings 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.
Books on the topic "Homeopathic materia medica"
Barthel, Horst. Characteristic of the homeopathic materia medica. Berg am Starnberger See, Germany: Barthel & Barthel, 1987.
Find full texttau, Max Te. Clinical homeopathic materia medica and biotherapeutic associations. Paris: Maloine, 1986.
Find full textMurphy, Robin. Homeopathic remedy guide: 1200 homeopathic and herbal remedies. Blacksburg, Va: H.A.N.A. Press, 2000.
Find full textJohnston, Linda. Repertory additions from Kent's homeopathic materia medica. 2nd ed. Los Angeles: Christine Kent Agency, 1990.
Find full textservice), SpringerLink (Online, ed. Materia Medica of New and Old Homeopathic Medicines. Berlin, Heidelberg: Springer-Verlag GmbH Berlin Heidelberg, 2012.
Find full textMurphy, Robin. Lotus materia medica: 1200 homeopathic and spagyric medicines. Pagosa Springs, Colo: Lotus Star Academy, 1995.
Find full textRiley, David S. Materia Medica of New and Old Homeopathic Medicines. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54192-0.
Full textRiley, David S. Materia Medica of New and Old Homeopathic Medicines. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-25292-1.
Full textShore, Jonathan. Birds: Homeopathic remedies from the avian realm. Berkeley, Calif: Homeopathy West, 2004.
Find full textJouanny, Jacques. The essentials of homeopathic therapeutics. 4th ed. Ste-Foy-lès-Lyon, France: Laboratoires Boiron, 1994.
Find full textBook chapters on the topic "Homeopathic materia medica"
Riley, David S. "Homeopathic Drug Provings." In Materia Medica of New and Old Homeopathic Medicines, 1–3. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54192-0_1.
Full textRiley, David S. "Homeopathic Drug Provings – An Introduction to General Methodological Considerations." In Materia Medica of New and Old Homeopathic Medicines, 1–3. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-25292-1_1.
Full textRiley, David S. "Benzochinonum, para-." In Materia Medica of New and Old Homeopathic Medicines, 59–60. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54192-0_17.
Full textRiley, David S. "Oleander." In Materia Medica of New and Old Homeopathic Medicines, 147–48. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-25292-1_50.
Full textRiley, David S. "Urtica urens." In Materia Medica of New and Old Homeopathic Medicines, 199–201. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-25292-1_66.
Full textRiley, David S. "Anthrachinon." In Materia Medica of New and Old Homeopathic Medicines, 29–31. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-25292-1_10.
Full textRiley, David S. "Arteria suis." In Materia Medica of New and Old Homeopathic Medicines, 33–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-25292-1_11.
Full textRiley, David S. "Ascophyllum nodosum." In Materia Medica of New and Old Homeopathic Medicines, 35–36. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-25292-1_12.
Full textRiley, David S. "Bacterium coli." In Materia Medica of New and Old Homeopathic Medicines, 37–39. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-25292-1_13.
Full textRiley, David S. "Barium oxalsuccinicum." In Materia Medica of New and Old Homeopathic Medicines, 41–42. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-25292-1_14.
Full textConference papers on the topic "Homeopathic materia medica"
Block, Janice. "19th Century Homeopathic Materia Medica Texts Predict Source Materials Whose Physiology Influences Thyroid Activity." In HRI London 2019—Cutting Edge Research in Homeopathy: Presentation Abstracts. The Faculty of Homeopathy, 2020. http://dx.doi.org/10.1055/s-0040-1702099.
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