Comparison between primary skin closure with drain and deleyed primary closure of wounds of perforation peritonitis- A randomized control trial
Not Applicable
- Conditions
- Health Condition 1: null- Patients with perforation peritonitis undergoing Exploratory laparotomy via midline incision.
- Registration Number
- CTRI/2020/02/023510
- Lead Sponsor
- Harjeet Singh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with perforation peritonitis undergoing Exploratory laparotomy via midline incision
Exclusion Criteria
Patients underwent Bagota closure or laparostomy at the time of surgery
American society of Anesthesiologist (ASA) score > 3 E (annexure)
Patients with previous midline laparotomy or scar
Patients with enterostomy over main wound
Patients not giving consent for study
Death of the patient on or before POD 6
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Superficial surgical site infectionTimepoint: Up to 30 day of hospital discharge
- Secondary Outcome Measures
Name Time Method facial dehiscence <br/ ><br>complete wound healing time <br/ ><br>total hospital stay <br/ ><br>cosmetic wound appearance <br/ ><br>incisinal hernia <br/ ><br>Timepoint: up to 3 month of hospital discharge