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:
2025-12-26 @ 10:32 AM
Ignite Modification Date:
2025-12-26 @ 10:32 AM
NCT ID:
NCT00371228
Eligibility Criteria:
Inclusion Criteria:
* Healthy women and their newborn infants delivered at Tulsa Regional Medical Center,
* between the ages of 18 and 34,
* full term (37 to 41 weeks),
* singleton pregnancy at the time of delivery
Exclusion Criteria:
* Delivery complicated by non-reassuring fetal heart tones,
* preeclampsia,
* eclampsia,
* chronic hypertension,
* meconium-stained amniotic fluid,
* fetal anomalies or
* any other condition which could require immediate newborn evaluation by nursery personnel at the time of delivery. Infants requiring operative delivery by forceps or vacuum also will be excluded.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
34 Years
Study:
NCT00371228
Study Brief:
Protocol Section:
NCT00371228