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Datura metel in Homoeopathy: Novel Therapeutic Insights from an Open-Label Multicenter Clinical Verification Study
Panaparambil Azis Suhana1, Meenu Gupta2, Jain Vij Shruti2
1Department of Clinical Verification, Central Council for Research in Homoeopathy, Ministry of Ayush, Government of India, New Delhi, India, suhanap@ccrhindia.nic.in.
Introduction:
Clinical verification in homoeopathy is a systematic scientific procedure that confirms the therapeutic utility of homoeopathic medicines. Despite its referencing in homoeopathic literature, Datura metel remains fragmentarily verified and rarely prescribed. To address this gap, the Central Council for Research in Homoeopathy (CCRH) conducted clinical verification of the medicine to assess its clinical utility and expand its therapeutic potential.
Methods:
A multicentric open-label single-arm study was carried out across the outpatient departments of the 14 health facilities of CCRH situated in various regions of India. Here, 341 participants with at least three symptoms corresponding to the proven symptomatology of D. metel were enrolled and prescribed the medicine. Response to treatment was assessed using validated outcome measures, namely, Measure Yourself Medical Outcome Profile-2 (MYMOP-2) and Outcome in Relation to Impact on Daily Living (ORIDL) scores. Additionally, the emergence of clinical symptoms after medicine administration was documented.
Results:
A statistically significant improvement was observed in the scores of MYMOP-2 and ORIDL scale (p < 0.0001****) of 211 participants who completed at least two follow-ups. The therapeutic action of this medicine was clinically verified across a range of common clinical conditions, including rhinitis, arthralgia, dyspepsia, dysmenorrhea, dermatitis, headache, and sinusitis. 'Pain in back' was found to be the most commonly reported clinical symptom during the study.
Conclusion:
This study is the first systematic effort to investigate the therapeutic attributes of the homoeopathic medicine D. metel and contributed to developing preliminary evidence on its clinical profile. Future research with more rigorous, in-depth, and controlled methodologies will contribute to build up the therapeutic profile of this medicine.
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