CTRI/2021/09/036872Not yet recruitingPhase 2
Comparative study of Virechana and Shamana Chikitsa in Vicharchika W.S.R to Eczema.
Dr Neha1 site in 1 country50 target enrollmentStarted: September 29, 2021Last updated:
Trial Snapshot
- Phase
- Phase 2
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 50
- Locations
- 1
- Primary Endpoint
- Assessed by change in the signs and symptoms of vicharchika
Study Overview
Brief Summary
Eczema patients will be selected according to signs and symptoms i.e 50 patients will be selected and divided into two groups each consists of 25 patients and conduct a clinical study to find whether is there any difference between Virechana procedure followed by Eladi lepa and followed by Navakashaya in the management of Vicharchika w.s.r to Eczema and evaluate the efficacy of virechana followed by Eladi lepa and followed by Navakashaya and compare the efficacy and safety of both.
Study Design
- Study Type
- Interventional
- Allocation
- Random Number Table
- Masking
- Open Label
Eligibility Criteria
- Ages
- 20.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patients willing for trial, diagnosed Eczema on the basis of signs & symptoms and fit for Virechana and Shamana treatment.
Exclusion Criteria
- •Patients less than 20 years & more than 60years,infected patch and pus collection, secondary infection, chronic diseases, malignancy, pregnant, lactating women and unfit patients for Virechana & Shamana treatment.
Outcomes
Primary Outcomes
Assessed by change in the signs and symptoms of vicharchika
Time Frame: 50 days
Secondary Outcomes
- Assessed by change in the objective parameters(50 days)
Investigators
Study Sites (1)
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