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.
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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

Anna AMORUSO

+3224773250

anna.amoruso@hubruxelles.be

CONTACT

Andrew CARLIN

+3224773295

andrew.carlin@chu-brugmann.be

CONTACT