Delayed Cord Clamping in Preterm Neonates
Completed · Not applicable
Conditions studied: Premature Birth of Newborn, Infant, Very Low Birth Weight, Delayed Separation of Umbilical Cord, Placental Transfusion
In brief
Delayed cord clamping (DCC) from 30 to 60 seconds allows blood to continue to flow from the placenta through the umbilical cord to the infant, thus resulting in a placental transfusion. This transfusion may improve circulating volume at birth leading to a smoother postnatal transition and overall improved outcome for preterm infants. The average blood volume delivered with DCC up to 90 seconds in preterm infants has been estimated to be about 12 ml per kg with vaginal deliveries resulting in slightly higher transfusions compared to cesarean deliveries. Several several short-term benefits have been described including a reduction in the need for blood transfusions as well as a possible reduction in intraventricular hemorrhage and necrotizing enterocolitis. All mothers with threatened preterm delivery between 28 and 34 6/7 weeks will be approached for the study. Following consent, the infant will be randomly assigned to either a 30 or 60 second delay in cord clamping in the delivery room. If the infant is not breathing by 30 seconds, the cord will be clamped and the infant moved to a resuscitation area. The primary outcome is a 3 percent difference in the hematocrit at one hour (routinely obtained on all babies). With approximately 75 neonates in each group (30 and 60 second DCC), there is 80% power to detect a difference in the mean hematocrit of 3% using a two-sample t-test with a 0.05 two-sided significance level.
Key facts
- Study ID
- NCT02478684
- Run by
- Weill Medical College of Cornell University
- People needed
- 105
- Starts
- 2015-07-01
- Expected to finish
- 2019-03-30
- Last updated by the study team
- 2019-10-30
Who can join
Age: 1 and older, up to 1. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Premature infants between 28 and 34 6/7 weeks
- Parents have given informed consent
You may not qualify if…
- Suspected placental abruption
- Bleeding from placenta previa
- Terminal bradycardia
- Cord prolapse
- Meconium
- Any major congenital anomalies
Where it is running
- Weill Cornell medical College — New York, New York, United States
Full record on ClinicalTrials.gov
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