Status:
COMPLETED
Neonatal Resuscitation With Intact Cord
Lead Sponsor:
Sharp HealthCare
Collaborating Sponsors:
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Conditions:
Intraventricular Hemorrhage
Eligibility:
All Genders
23-31 years
Phase:
NA
Brief Summary
The purpose of this study is to examine whether providing ventilation during delayed umbilical cord clamping provides greater placental transfusion and improved hemodynamic transition at birth.
Detailed Description
Subjects will receive 1 minute of delayed cord clamping in both arms. One arm will receive routine care, warm dry and stimulate during the 1 minutes transfusion. The second arm will receive routine ca...
Eligibility Criteria
Inclusion
- Gestational Age: Women admitted 23+0 to 31+6 weeks (Reason: Highest risk for IVH)
Exclusion
- Gestational Age: Parents decline consent (Reason: Can only perform intervention at time of delivery)
- Congenital anomalies of newborn (Reason: Exclude the effect of abnormal hematological function)
- Placental abruption (Reason: Exclude pregnancies at risk for hemorrhage at the time of delivery)
- Twin to twin transfusion (Reason: Exclude possible loss of blood from other twin during delayed cord clamping)
- Placenta Accreta
- Prolonged premature rupture of membranes (\> 2 weeks) prior to 23 weeks gestation
Key Trial Info
Start Date :
August 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2016
Estimated Enrollment :
150 Patients enrolled
Trial Details
Trial ID
NCT02231411
Start Date
August 1 2014
End Date
August 1 2016
Last Update
May 30 2017
Active Locations (1)
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1
Sharp Mary Birch Hospital for Women and Newborns
San Diego, California, United States, 92123