homoeopathy; pathogenetic effect; homoeopathic pathogenetic trial; drug proving; Bacopa monnieri
Objective: To elicit the pathogenetic response of the drug Bacopa monnieri in homoeopathic potencies on healthy human beings. Methodology: Drug Bacopa monnieri was proved by the Central Council for Research in Homoeopathy through randomized, double-blind, placebo-controlled method. The study was conducted at two centers. The drug was proved in three potencies (6C, 30C and 200C) on 32 apparently healthy volunteers who were selected after conducting pre-trial medical examination by the medical specialists and routine laboratory investigations. In the first phase volunteers were given 56 doses (04 doses per day for 14 days) of placebo. In the next three phases 56 doses (04 doses per day for 14 days) of each potency or placebo were consumed. The symptoms generated during the trial period were noted by the volunteers and elaborated by the Proving Masters. The data obtained from both the centers was compiled at provingcum- data processing cell at CCRH headquarters after de-coding. Observations: Out of the 20 provers who were on actual drug trial, 07 manifested symptoms. Drug was able to produce symptoms in all three potencies more or less related to every part of the body. Conclusion: The pathogenetic responses elicited during the proving trial expands the scope of use of the drug Bacopa monnieri and will benefit the research scholars and clinicians. These symptoms will carry more value when verified clinically.
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Wolters Kluwer India Pvt. Ltd.
How to cite this article
Rajpal R, Singh V, Siddiqui V, Nayak C, Mal P, Sarkar D. Bacopa monnieri - A multicentric, randomized, double-blind homoeopathic pathogenetic trial. Indian J Res Homoeopathy 2011;5(4):22-27. doi: 10.53945/2320-7094.1732