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 @ 4:14 AM
Ignite Modification Date:
2025-12-25 @ 4:14 AM
NCT ID:
NCT00009620
Eligibility Criteria:
Inclusion Criteria:
* Admission to a high risk perinatal unit or labor and delivery unit;
* 24 to 32 completed weeks gestation;
* Expected delivery within 24 hrs;
* Preterm labor or no labor with planned delivery for maternal-fetal indications;
Exclusion Criteria:
* Anticipated delivery within two hours
* Multiple congenital or chromosomal abnormalities in the fetus
* Multiple gestation with more than two fetuses
* Administration of phenobarbital during the pregnancy
* Administration of indomethacin within one week before admission
* Maternal platelet count of less than 100,000 per cubic millimeter
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT00009620
Study Brief:
Protocol Section:
NCT00009620