Relaparotomy Study - A prospective analysis of the standard of care and outcomes of patients undergoing relaparotomy with one randomized step (fascial closure)
Phase 3
- Conditions
- Abdominal re-operationsPrimary laparotomy
- Registration Number
- DRKS00013001
- Lead Sponsor
- niversitätsklinikum Heidelberg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 181
Inclusion Criteria
experimental group: relaparotomy of every kind, not depending on the underlying disease; control group: primary laparotomy of every kind, not depending on the underlying desease
Exclusion Criteria
primary reason of the relaparotomy is an incisional hernia or laparostoma; surgery in retroperitoneum without transperitoneal acces, urgency operation; underaged or non-compliant patient
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method