CTRI/2019/06/019515CompletedPhase 1
Homoeopathic drug proving: Randomized double blind placebo controlled trial for drug code 120
Central Council for Research in Homoeopathy0 sites88 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 1
- Status
- Completed
- Sponsor
- Enrollment
- 88
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1. Healthy individuals with no apparent disease and normal routine laboratory parameters during screening
- •2. Healthy individuals identified as fit for proving by experts
- •3. Intelligent enough to record carefully the facts, subjective and objective symptoms generated by the IPS during proving.
- •4. Able to be informed of the nature of the study and willing to give written informed consent.
Exclusion Criteria
- •1. 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
- •2. Persons with colour blindness.
- •3. Persons who have undergone surgery in last two months.
- •4. 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.
- •5. Volunteers on regular medication (allopathic, ayurvedic, homoeopathic, naturopathic, unani, etc.) for any acute or chronic disease.
- •6. 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.
- •7. Emotionally disturbed, hysterical or anxious persons.
- •8. Persons having known history of allergies, food hypersensitivity, etc.
- •9. Women during pregnancy, puerperium and while breast-feeding and women who have undergone hysterectomy.
- •10. Smokers who smoke more than 10 cigarettes per day
- •11. Recent history of alcoholism / drug addictions or unlikely to refrain from excessive alcohol consumption / drug intake during the study period
- •12.Participation in another clinical or proving trial during the last 6 months
Investigators
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