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

Not yet recruiting

• Conditions: Intestinal malabsorption, unspecified. Ayurveda Condition: GRAHANIDOSHAH,

• Registration Number: CTRI/2021/04/032523
• Lead Sponsor: dr d y patil patil vidyapeeth pune

Brief Summary

30 patients will be taken for clinical trial

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2021-01-04
• Study Start: 2021-08-04

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 30

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 Syndrome	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 procedure	at start of trial and end of trial i.e. on 1st day and 8th day of trial

Trial Locations

Locations (1)

dr d y patil vidyapeeth pune; 🇮🇳 Pune, MAHARASHTRA, India

dr d y patil vidyapeeth pune

🇮🇳Pune, MAHARASHTRA, India

dr mamata nakade

Principal investigator

9850241887

mamta.nakade@dpu.edu.in