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The main aim of the study is to determine whether a homeopathic drug in the potency C12 provokes more characteristic homeopathic proving symptoms after three weeks compared to a placebo in healthy volunteers.
Secondary aims are to develop and to test a qualitative analysis methodology on which to base a definition for drug-specific (characteristic) symptoms and to compile a profile of characteristic homeopathic proving symptoms of the drug being trialled for therapeutic purposes.
This study protocol adapts the traditional homeopathic drug proving methodology to a modern clinical trial design.
Allocation: Randomized, Control: Placebo Control, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Homeopathic drug C12, Placebo
Not yet recruiting
Charite University, Berlin, Germany
Published on BioPortfolio: 2014-08-27T03:16:13-0400
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Authoritative resources describing the composition, properties, manufacture, and quality control of HOMEOPATHIC REMEDIES.
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Formularies concerned with HOMEOPATHIC REMEDIES.
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