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 @ 7:45 PM
Ignite Modification Date:
2025-12-24 @ 7:45 PM
NCT ID:
NCT02092103
Eligibility Criteria:
Inclusion Criteria:
* Admitted to Labor \& Delivery at Good Samaritan TriHealth Hospital in Cincinnati, Ohio with expected/possible preterm delivery between 23-34 weeks gestation
* Care provided by Good Samaritan TriHealth Hospital's Faculty Medical Center or Tri-State Maternal Fetal Medicine
Exclusion Criteria:
* Declined to participate
* Known congenital anomalies
* Precipitous delivery preventing completion of the protocol
* Placental abruption around the time of or as indication for delivery
* Mother has uterine rupture
* Non reassuring fetal heart tracing (FHT) immediately prior/leading to delivery
* Multiple gestation
* Parvo B19
* Infants known to be at risk of anemia due to isoimmunization (mother has red blood cell antibodies
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT02092103
Study Brief:
Protocol Section:
NCT02092103