Effect of Vamana Dhauti In The Management of Amlapitta- An Exploratory Open Clinical Trial
Trial Snapshot
- Phase
- Phase 2
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 20
- Locations
- 1
- Primary Endpoint
- There may be a good reduction in symptomatology of the patient even with the non-pharmacological intervention, so that, the burden of everyday medication could be minimised or reduced to nil.
Study Overview
Brief Summary
Amlapitta adversely affects the quality of life of patients, making it difficult to make dietary choices and causing insomnia even hampering social life and contributes to medical expenses. So, considering the above factors, the clinical study will be conducting to assess the effect of Vamana dhauti, one among the purification procedures explained for upper gastro-intestinal tract, which is very simple to administer, cost effective and feasible in all seasons.
Study Design
- Study Type
- Interventional
- Allocation
- Computer generated randomization
- Masking
- Not Applicable
Eligibility Criteria
- Ages
- 21.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •1 Patients fit for Vamana Dhauti 2 Known cases of Amlapitta.
Exclusion Criteria
- •1 Known cases of peptic ulcer, duodenal ulcer, carcinoma stomach, cardiac disorders, hypertension, diabetes mellitus, and chronic renal failure.
- •2 Pregnant and lactating women.
Outcomes
Primary Outcomes
There may be a good reduction in symptomatology of the patient even with the non-pharmacological intervention, so that, the burden of everyday medication could be minimised or reduced to nil.
Time Frame: 18 months
Secondary Outcomes
- Analysis of the vaanta dravya (Vomitus) for its Organo-leptic and Physico-chemical properties(18 months)
