CTRI/2024/09/073743Not yet recruitingPhase 2
A comparative pharmaceutical analytical study of balachaturbhdra churna with its another dosage form i.e.balachaturbhdra avaleha with special reference to kasa in children
Government Ayurvedic College and Hospital chaukaghat Varanasi1 site in 1 country60 target enrollmentStarted: September 30, 2024Last updated:
Trial Snapshot
- Phase
- Phase 2
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- Improvement in kasa
Study Overview
Brief Summary
Interventional study
Patient suffering from kasa will selected from opd of government Ayurvedic College and Hospital chaukaghat Varanasi
Total patient=60
Treatment plan
Group A-30 patient will be treated with Balachaturbhdra churna
Group B-30 patient will be treated with Balachaturbhdra avaleha
Study Design
- Study Type
- Interventional
- Allocation
- Coin toss, Lottery, toss of dice, shuffling cards etc
- Masking
- None
Eligibility Criteria
- Ages
- 3.00 Year(s) to 16.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patients of either gender, caste, socio-economic status etc.
- •With age group 3 to 16 year Patients having classical clinical signs and symptoms of kasa Patients having a complaint history within one month.
Exclusion Criteria
- •Patients having age below 3 year Patients having age above 16 year Individuals suffering from systemic pathologies like SLE, Cancer, severe hormonal imbalance and tuberculosis AIDS etc severe skin infection or allergies etc.
- •Patients on medication of Hormonal Therapy.
Outcomes
Primary Outcomes
Improvement in kasa
Time Frame: 4 weeks
Secondary Outcomes
- Improvement in other symptoms(14 to 16 days)
Investigators
Dr sangeeta pal
Government Ayurvedic College and Hospital, chaukaghat, Varanasi
Study Sites (1)
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