About this trial
This randomized controlled trial aims to evaluate the efficacy of preoperative vaginal cleansing with 5% povidone-iodine in reducing postoperative infectious morbidity among women undergoing cesarean section. The primary outcomes include wound-related complications, while secondary outcomes include postoperative fever, endometritis, wound infection, and white blood cell count.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
None
Disqualifiers
Active infection No prophylactic antibiotics Chorioamnionitis Placenta previa with antepartum hemorrhage
Trial design
Parallel
Treatments tested in this trial
Povidone-iodine 5% solution
DrugVaginal cleansing with 5% povidone-iodine for 30 seconds before cesarean section.
Treatment groups
Trial outcomes
Primary outcomes
Incidence of postoperative wound-related complications Time Frame: Within 8 weeks after cesarean section
Incidence of postoperative wound-related complications
Secondary outcomes
Postoperative fever (within 8 weeks) Postoperative WBC count (24 hours) Endometritis (within 8 weeks) Combined wound complications and endometritis
Sponsors and contacts
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Mohamed Mousa Mohamed Mousa
Lead sponsor
Al-Azhar University
Sponsor institution
This trial is not recruiting at the moment. You can still explore other options: