Additional injection to prevent infection after cesearean delivery
Phase 3
Completed
- Conditions
- Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperiumHealth Condition 2: null- Pregnant women completed 37 weeks undergoing cesarean section
- Registration Number
- CTRI/2015/10/006329
- Lead Sponsor
- internal fluid research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 2000
Inclusion Criteria
pregnant women with completed 37 weeks undergoing cesarean section
Exclusion Criteria
Patients with known allergy to Cephalosporin and Azithromycin
Patient who have received antibiotics within a week prior to the delivery or intrapartum propylaxis for chorioamnionitis.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method