Clinical Trial

Effect of Betadine Vaginal Cleansing Before Cesarean Section to Reduce Postoperative Infectious Morbidity

Not Yet Recruiting
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Summary
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.
Trial Details
NCT Number NCT07715409
Lead Sponsor Mohamed Mousa Mohamed Mousa
Conditions Cesarean Section, Surgical Site Infection, Endometritis
Enrollment 600 participants
Start Date 2027-05-01
Primary Completion 2027-05-01 (estimated)
Study Completion 2027-05-01 (estimated)
Updated on ClinicalTrials.gov 2026-07-20