CTRI/2024/03/064237Not yet recruitingPhase 1
Homoeopathic Drug Proving of Drug Code 160: A Multicentre, double blind, randomized placebo controlled trial. - NI
Central Council for Research in Homoeopathy0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 1
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •Age : 18 – 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
- •Any disease or condition which might compromise the hematopoietic, renal, endocrine, pulmonary, central nervous system, cardiovascular, immunological, dermatological, gastro-intestinal or any other body system.
- •Persons with colour blindness.
- •Persons who have undergone surgery in last two months.
- •Planned medical / dental treatment during the proving period including herbal or dietary supplements, procedures, or medications that are likely to interfere with, or substantially alter, responsiveness to the proving substance.
- •Volunteers on regular medication (allopathic, ayurvedic, homoeopathic, naturopathic, unani, etc.) for any acute or chronic disease.
- •Participant must not be on any homoeopathic remedy in the preceding one month and have had no significant change in health status in last one month.
- •Emotionally disturbed, hysterical or anxious persons.
- •Persons having known history of allergies, food hypersensitivity, etc.
- •Women during pregnancy, puerperium and while breast-feeding and women who have undergone hysterectomy.
- •Smokers who smoke more than 10 cigarettes per day.
- •Recent history of alcoholism / drug addictions or unlikely to refrain from excessive alcohol consumption / drug intake during the study period
- •Participation in another clinical or proving trial during the last 6 months.
Investigators
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