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 @ 3:46 AM
Ignite Modification Date:
2025-12-25 @ 3:46 AM
NCT ID:
NCT02409602
Eligibility Criteria:
Inclusion Criteria:
* 18-35 year-old women who underwent bilateral internal iliac artery ligation (BIIAL) due to postpartum hemorrhage
* Age-matched healthy puerperal women
Exclusion Criteria:
* Known Diabetes Melitus or cardiovascular disease
* Known affection disorder before or during pregnancy
* B-lynch procedure, ligation of uterine or ovarian artery, hysterectomy and salphingooophorectomy following postpartum hemorrhage
* Known functional sexual disorder before pregnancy
* Postoperative endometritis or other puerperal infections
* Postoperative thromboembolic incidence
* Cessation of breastfeeding in puerperal period
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT02409602
Study Brief:
Protocol Section:
NCT02409602