Effect of Betadine Vaginal Cleansing Before Cesarean Section to Reduce Postoperative Infectious M… (NCT07715409) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effect of Betadine Vaginal Cleansing Before Cesarean Section to Reduce Postoperative Infectious Morbidity
Egypt600 participantsStarted 2027-05-01
Plain-language 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.
Who can participate
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
\- Women undergoing elective or emergency cesarean section. Received prophylactic antibiotics before surgery
Exclusion Criteria:
* Active infection No prophylactic antibiotics Chorioamnionitis Placenta previa with antepartum hemorrhage
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial is testing whether a Betadine vaginal wash before a cesarean section can reduce infections like wound complications and endometritis — is this something my care team already does, or would joining this study be the only way I'd receive it?
2Since this trial isn't recruiting yet, do you know when it's expected to open, and would waiting to enroll affect the timing of my planned cesarean section?
3The study follows patients for up to 8 weeks after the cesarean — what does that follow-up look like in terms of extra visits or check-ins, and is that realistic given my situation after delivery?
4Are there any known risks or sensitivities I should be aware of with Betadine used vaginally, especially if I have allergies or certain skin conditions, before I consider whether this trial might be appropriate for me?
5Outside of this trial, what does current evidence say about preventing surgical site infections and endometritis after a cesarean, so I can understand how this approach compares to what would be standard care for me?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Incidence of postoperative wound-related complications Time Frame: Within 8 weeks after cesarean section
Timeframe: 8 weeks
2
Incidence of postoperative wound-related complications
Timeframe: Within 8 weeks after cesarean section
Trial details
NCT IDNCT07715409
SponsorMohamed Mousa Mohamed Mousa
Sponsor typeOTHER
Study typeINTERVENTIONAL
Primary completion2027-05-01
Contact for this trial
mohamed mousa Al-Azhar University Hospital, Damietta