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 @ 3:49 PM
Ignite Modification Date:
2025-12-24 @ 3:49 PM
NCT ID:
NCT01180192
Eligibility Criteria:
Inclusion Criteria:
* gestational age between 37 and 42 weeks;
* singleton pregnancy;
* live fetus;
* cephalic presentation;
* neonatal birth weight of 2500-4500 g;
* parity between one and five;
* maternal age \< 35 years old;
* vaginal birth
Exclusion Criteria:
* blood pressure ≥ 140/90mmHg;
* placenta previa;
* placental abruption;
* a history of any bleeding during pregnancy;
* a history of curettage;
* cesarean section or any uterine scar;
* a history of postpartum hemorrhage;
* polyhydramnios;
* signs or symptoms of maternal infection;
* known uterine anomalies;
* history of any drug use during labor;
* abnormal placentation;
* coagulation defects;
* instrumental deliveries;
* hemoglobin concentration \< 8 g/dL;
* history of anticoagulant drugs;
* beta-mimetic medications during pregnancy;
* prolongation of the first stage of labor \> 15 hours
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
40 Years
Study:
NCT01180192
Study Brief:
Protocol Section:
NCT01180192