Physiologically Based Cord Clamping To Improve Neonatal Outcomes In Moderate And Late Preterm Newborns
Recruiting
N/A
Interventional Study
Premature Birth
Respiratory Distress Syndrome in Premature Infant
Sepsis
Intraventricular Hemorrhage of Prematurity
Bronchodysplasia
Jaundice
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 32 Weeks – 36 Weeks
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 180 (estimated)
- Sponsor
- Queen Fabiola Children's University Hospital · Other
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About This Trial
Before birth, the baby's lungs are filled with fluid and babies do not use the lungs to breathe, as the oxygen comes from the placenta. As delivery approaches, the lungs begin to absorb the fluid. After vaginal delivery, the umbilical cord is clamped and cut after a delay that allows some of the blood in the umbilical cord and placenta to flow back into the baby. Meanwhile, as the baby breathes fo…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
Pregnant women followed-up in Brugmann University Hospital will be eligible to participate if:
* The delivery takes place between 32 0/7 and 36 6/7 weeks of gestation
* They carry singletons
Exclusion Criteria:
* Fetal anomalies including congenital malformations, anemia, and…
Contacts