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 @ 5:03 AM
Ignite Modification Date:
2025-12-25 @ 5:03 AM
NCT ID:
NCT02733718
Eligibility Criteria:
Inclusion Criteria:
* Prematurity (\<32 completed weeks of gestation at birth)
* Need for PRBC transfusion
* Feeding at least 30ml/kg/day at the time of transfusion
Exclusion Criteria:
* Neonates previously diagnosed with gastrointestinal problems such as NEC, intestinal perforation or atresia.
* Infants receiving continuous feeds or less than 30ml/kg/day
* Major congenital or chromosomal abnormalities or infants unlikely to survive
* Intraventricular hemorrhage \>Grade 3
* Hemodynamically significant patent ductus arteriosus
* Infants requiring vasopressor support
* Skin disruption precluding application of sensors
Healthy Volunteers:
False
Sex:
ALL
Maximum Age:
4 Months
Study:
NCT02733718
Study Brief:
Protocol Section:
NCT02733718