Evaluation of surgical site infection bundle to decrease infectious in women undergoing caesarean sectio
Not Applicable
Completed
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indication
- Registration Number
- CTRI/2019/01/017110
- Lead Sponsor
- Megha jindal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 202
Inclusion Criteria
1. Emergency caesarean section
2. Patients with caesarean section beyond 28 weeks of gestation
3. Patient with Pfannensteil incision and midline vertical incision
Exclusion Criteria
1. Patients with classical caesarean section
2. Patients with pre-existing skin infection e.g. Taenia, Scabies
3. Patients with Diabetes Mellitus, Gestational diabetes
4. Immunosuppressed patients
5. Patient on steroid therapy
6. Patients with premature rupture of membranes
7. Patients with pre-existing sepsis
8. Patient with known connective tissue disorders
9. Patients with morbid obesity (BMI >40kg/m2 )
10. Patients with severe anaemia (Hb < 7g/dl)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the effects of preoperative skin preparation, use <br/ ><br>of closing pans and appropriate antibiotic dosing schedule on post-operative <br/ ><br>infectious morbidity like fever, wound healing, duration of hospital stay <br/ ><br>amongst emergency lower segment caesarean section cases.Timepoint: 48 hr, day 8 and day 30
- Secondary Outcome Measures
Name Time Method To evaluate duration of surgery and type of organism <br/ ><br>grown in wound culture in patients with surgical site infection.Timepoint: 2