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:
2025-12-24 @ 2:54 PM
Ignite Modification Date:
2025-12-24 @ 2:54 PM
NCT ID:
NCT02414659
Eligibility Criteria:
Inclusion Criteria:
* Elective cesarean deliveries
* Women with a blood count results maximum 30 days prior to delivery
Exclusion Criteria:
* Emergent cesarean deliveries
* Cesarean deliveries due to placental adhesion abnormalities or placenta previa
* Patients on anticoagulation regimens
* Postpartum bleeding due to uterine atony, retained placenta
* Patients with a history of bleeding 30 days prior to delivery
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT02414659
Study Brief:
Protocol Section:
NCT02414659