Clinical Trials Directory

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UnknownNCT00562536

Delayed Umbilical Cord Clamping in Infants Less Than 32 Weeks

Delayed Umbilical Cord Clamping in Infants Less Than 32 Weeks: A Randomized Controlled Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
296 (estimated)
Sponsor
Mount Sinai Hospital, Canada · Academic / Other
Sex
Female
Age
15 Years – 50 Years
Healthy volunteers
Accepted

Summary

The overall objective of the present study is to examine the effects of delayed umbilical cord clamping in preterm infants on neonatal outcomes using a prospective randomized controlled trial comparing immediate cord clamping (standard at present) with delayed cord clamping. Our specific aim is to determine if a 30 to 45 second delay in umbilical cord clamping improves neonatal outcome as assessed by a composite of intraventricular hemorrhage and late onset sepsis in preterm infants born between 24 and 32 weeks gestation. Secondary outcomes to be examined include improvements in the following: 1) lung function as assessed by oxygen dependency at 36 weeks corrected gestational age (CGA), 2) cardiovascular function as assessed by the need for volume expansion, inotropes, or clinically suspected PDA requiring intervention prior to discharge home, and 3) anemia as assessed by initial hemoglobin, need for transfusion during stay in the NICU, and number of transfusions.

Conditions

Interventions

TypeNameDescription
PROCEDUREUmbilical cord clampingDelay of umbilical cord clamping 30 to 45 seconds

Timeline

Start date
2007-11-01
Completion
2010-11-01
First posted
2007-11-22
Last updated
2007-11-22

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00562536. Inclusion in this directory is not an endorsement.