To study the Role of bioresorbable membranes in patients undergoing abdominal surgeries by placing this membrane in the abdominal cavity which will reducie the post operative adhesions formed leading to decrease in incidence of intestinal obstructions and the bowel injury during redosurgeries
Phase 2
- Conditions
- Health Condition 1: K639- Disease of intestine, unspecified
- Registration Number
- CTRI/2024/05/066860
- Lead Sponsor
- PGIMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patient giving consent for the study who will undergo a temporary stoma formation in which stoma closure would be done in 6-8weeks
Exclusion Criteria
Permanent stoma formation.
Patient with prior history of abdominal TB and inflammatory bowel disease.
Patients in which stoma reversal is not possible in 6-8weeks
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To study the role of this bioresorbable membrane in reducing the severity of postoperative intraabdominal adhesionsTimepoint: During 2nd surgery i.e 6-8 weeks post index surgery
- Secondary Outcome Measures
Name Time Method To study the decrease in operating time during surgery for stoma reversalTimepoint: During 2nd surgery i.e 6-8weeks post index surgery