A clinical trial to study the efficacy of delayed skin suturing in minimising wound infection in cases of gut perforatio
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Perforative peritonitis
- Registration Number
- CTRI/2018/02/011973
- Lead Sponsor
- Medical College Kolkata
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
All patients undergoing surgical intervention for perforative peritonitis after taking informed consents
Exclusion Criteria
1. Immunocompromised patients
2. Patients with pre-existing skin infection
3. Patients not willing to participate in the study
4. Patients having diabetes mellitus or chronic renal failure
5. Patients taking immunosuppressive therapy for other causes
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of superficial surgical site infectionTimepoint: 30 days post-operatively
- Secondary Outcome Measures
Name Time Method ength of hospital stayTimepoint: Days