A randomised controlled study to compare the effect of antibiotic infiltration at the incision site, in preventing surgical site infections in emergency midline surgeries.
Not Applicable
Completed
- Conditions
- Health Condition 1: - Health Condition 2: K631- Perforation of intestine (nontraumatic)Health Condition 3: K631- Perforation of intestine (nontraumatic)
- Registration Number
- CTRI/2020/07/026302
- Lead Sponsor
- MAULANA AZAD MEDICAL COLLEGE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
All patients diagnosed with perforation peritonitis.
Exclusion Criteria
Diabetes Mellitus.
On immunosuppresive therapy.
BMI > 35 Kg/m2
Sensitivity to ceftriaxone.
Previous midline abdominal surgery.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Effect of ceftriaxone infiltration before incision and before closure in preventing SSITimepoint: Effect of ceftriaxone infiltration before incision and before closure in preventing SSI on postoperative day 7.
- Secondary Outcome Measures
Name Time Method Duration of hospital stay.Timepoint: Time duration