Skip to content

To find out the pathogenetic effects of BSC-022 on healthy volunteers.

Homeopathic drug proving: Randomized, double-blind, placebo-controlled trial of BSC-022 - BSC-022

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/043392
Enrollment
40
Registered
2022-06-21
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

None listed

Interventions

Intervention1: BSC-022: BSC-022 30c pills Dose: One dose of 6 pills per day for 2 weeks. Control Intervention1: Placebo: Placebo 30c pills Dose: One dose of 6 pills per day for 2 weeks.

Sponsors

Dr Rajesh Shah
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy individuals with no apparent disease and normal routine laboratory parameters during screening. 2. Intelligent enough to carefully record the facts, subjective and objective symptoms generated by the drug during proving. 3. Able to be informed of the nature of the study and willing to give written informed consent.

Exclusion criteria

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. COVID 19 RT-PCR positive individuals. 3. Persons with color blindness. 4. 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. 5. Volunteers on regular medication (allopathic, ayurvedic, Homeopathic, naturopathic, unani, etc.) for any acute or chronic disease. 6. Participant must not be on any Homeopathic 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. 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.

Design outcomes

Primary

MeasureTime frame
Symptoms experienced by provers will be recorded.Timepoint: Symptoms experienced by provers will be recorded daily for 7 weeks.

Secondary

MeasureTime frame
Safety parameters - including blood investigations ECG and X rayTimepoint: Disappearance of symptoms which appeared during the proving and subsequent symptom (significant symptoms) free period of 15 days.

Countries

India

Contacts

Public ContactDr Samit Ghosh

Dr. Samit Ghosh Clinic

drsamitghosh@gmail.com8910092118

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 6, 2026