Clinical study to find the effect of Takra basti for duration of 8 days along with panchamruta parpati in the management of irritable bowel syndrome (I.B.S.)
Phase 2
- Conditions
- Health Condition 1: K909- Intestinal malabsorption, unspecified
- Registration Number
- CTRI/2021/04/032523
- Lead Sponsor
- dr d y patil patil vidyapeeth pune
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
patients with irritable bowel syndrome
Exclusion Criteria
patients suffering from any other systemic disorders
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Relieving signs and symptoms of Irritable Bowel SyndromeTimepoint: before start of trial and end of trial i.e. on 1st day and 8th day of trial
- Secondary Outcome Measures
Name Time Method standardized the Takra Basti procedureTimepoint: at start of trial and end of trial i.e. on 1st day and 8th day of trial