Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2026-03-26 @ 3:19 PM
Ignite Modification Date:
2026-03-26 @ 3:19 PM
NCT ID:
NCT07474194
Eligibility Criteria:
Inclusion Criteria:
* female participants with singleton pregnancies scheduled for elective cesarean sections at term, specifically between 37 and 40 weeks of gestation
* free from any medical disorders.
* The participants' ages ranged from 18 to 40 years
* body mass index (BMI) ranged from 18 to 30 kg/m2
Exclusion Criteria:
1. Cases of urgent or emergent CS.
2. Abnormal vaginal secretion (bad smelling yellowish secretion, whitish cheesy discharge with pruritus, bloody discharge; etc…).
3. Women with medical disorders such as pre-gestational diabetes, anemia, hypertension, preeclampsia, or immunosuppressant pregnant women.
4. Women who had a skin infection adjacent to the operative site.
5. Allergy to topical povidone-iodine or clindamycin
6. Feverish patients or history of premature rupture of membranes or with placenta previa.
7. patients lost during follow-up were excluded from the final analysis.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
40 Years
Study:
NCT07474194
Study Brief:
Protocol Section:
NCT07474194