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:
2025-12-25 @ 12:20 AM
Ignite Modification Date:
2025-12-25 @ 12:20 AM
NCT ID:
NCT07228858
Eligibility Criteria:
Inclusion Criteria:
* ≥1 prior cesarean section at ≥28 weeks' gestation.
* Undergoing repeat cesarean section for any indication.
* Provided informed consent and agreed to 6-month postpartum follow-up.
* Not planning pregnancy during follow-up.
Exclusion Criteria:
* Uterine fibroids, multiple gestation, chorioamnionitis, placenta previa, placental abruption, or preeclampsia/eclampsia.
* Hepatic or renal dysfunction, uncontrolled diabetes, or hemoglobin \<10 g/dL.
* Systemic uncontrolled disease, chronic corticosteroid use, or smoking.
* Inability to provide informed consent.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT07228858
Study Brief:
Protocol Section:
NCT07228858