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 @ 1:46 AM
Ignite Modification Date:
2025-12-25 @ 1:46 AM
NCT ID:
NCT04827394
Eligibility Criteria:
Inclusion Criteria:
* Patients who have non-emergent cesarean deliveries (defined as at least 2 hours prior to planned cesarean)
* Gestational age between 32 weeks and 0 days and 36 weeks and 6 days determined per usual clinical parameters
Exclusion Criteria:
* Fetal anomalies or death
* Maternal diabetes
* Neonates with blistering skin conditions
* Reversed end diastolic umbilical artery flow
* Placental abruption
* Chorioamnionitis
* Monochorionic multifetal pregnancies
* Inability to provide consent
* Provider perception that patient is in significant pain and provider perceived contraindications to delayed cord clamping.
Healthy Volunteers:
False
Sex:
FEMALE
Maximum Age:
55 Years
Study:
NCT04827394
Study Brief:
Protocol Section:
NCT04827394