Effect of topical cefazolin on reducing cesarean section infectio
Phase 3
- Conditions
- Infection Caesarean section.Infection of obstetric surgical wound
- Registration Number
- IRCT2017092436376N1
- Lead Sponsor
- Vice chancellor for research, Sabzevar University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 108
Inclusion Criteria
women; Gestational age; Having a living and single fetus; Absence of underlying illness; Classic cesarean section (van Steele); Lack of rupture of the Amniotic sac
Exclusion criteria: Women under the age of 18 and over 40 years; Gestational age below 37 weeks; Stillbirth; History of underlying disease; Addiction; Recent antibiotic use; bleeding more than usual during cesarean section; non-classic cesarean sections; Rupture of the Amniotic sac longer than 18 hours
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Redness. Timepoint: Days 5 and 10. Method of measurement: Red spot on both sides of the wound.;Edama. Timepoint: Days 5 and 10. Method of measurement: Check swelling of the wound and measure to cm.;Ecchymosis. Timepoint: Days 5 and 10. Method of measurement: Check ecchymosis of the wound and measure to cm.;Discharge. Timepoint: Days 5 and 10. Method of measurement: observation.;Approximation. Timepoint: Days 5 and 10. Method of measurement: observation.
- Secondary Outcome Measures
Name Time Method Pain. Timepoint: Days 1, 5 and 10. Method of measurement: Measuring the severity of pain based on fatigue from 1 to 5.