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:
NCT07401160
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women aged 18-49 years.
* Singleton pregnancy.
* Gestational age ≥37 weeks.
* active labor with cephalic presentation.
* Planned for vaginal delivery.
* Capable of providing informed consent.
Exclusion Criteria:
* Planned or emergent cesarean section.
* Instrumental delivery (e.g., forceps, vacuum).
* Antepartum hemorrhage.
* Severe anemia (Hemoglobin \<8 g/dL) or specific hematological disorders (e.g., sickle cell disease, thalassemia, hemophilia, thrombocytopenia \<100,000/µL).
* Use of anticoagulant medication.
* Non-cephalic fetal presentation (e.g., breech, transverse).
* Refusal to participate or inability to provide informed consent.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
49 Years
Study:
NCT07401160
Study Brief:
Protocol Section:
NCT07401160