se of Isphagula for reducing stoma output
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/11/059917
- Lead Sponsor
- All India Institute of Medical Sciences, Bhubaneswar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients more than 18 years with ileostomy or jejunostomy with high output
Exclusion Criteria
Patients who cannot take orally, persistent nausea, vomiting or any contraindications to Isphagula.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Daily stoma output in each group upto 30 days or less if closed earlyTimepoint: 30 days/ till the stoma closure if closed earlier
- Secondary Outcome Measures
Name Time Method Stoma relied complicationsTimepoint: 30 days or till stoma closure, whichever is earlier