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Drug Proving of homoeopathic drug substance on healthy volunteers to elicit the effect of the drug on the health status.

Homoeopathic Pathogenetic Trial of Drug Code 167: A Multicentre, double blind, randomized placebo controlled trial. - NIL

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/107924
Enrollment
45
Registered
2026-04-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Drug code 167: To be administered in 30C, 200C and 1M potencies. 12 doses for each potency, frequency- four times a day for a maximum of 3 days, route of administration- oral. Control I

Sponsors

Central Council for Research in Homoeopathy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age : 18 to 60 years. Both males and females. Healthy individuals with no apparent disease and normal routine laboratory parameters during screening. Intelligent enough to record carefully the facts, subjective and objective symptoms generated by the drug during proving. Able to be informed of the nature of the study and willing to give written informed consent.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The pathogenetic effect of Drug Code 167 in form of signs and/or symptoms.Timepoint: At baseline and at the end of the trial.

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Pritha Mehra

Central Council for Research in Homoeopathy

drpritha@gmail.com9999036871

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026