Neonatal Resuscitation With Intact Cord

Completed · Not applicable

Conditions studied: Intraventricular Hemorrhage

In brief

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.

Key facts

Study ID

NCT02231411

Run by

Sharp HealthCare

People needed

150

Starts

2014-08-01

Expected to finish

2016-08-01

Last updated by the study team

2017-05-30

Who can join

Age: 0 and older, up to 1. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Gestational Age: Women admitted 23+0 to 31+6 weeks (Reason: Highest risk for IVH)

You may not qualify if…

• 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

Where it is running

• Sharp Mary Birch Hospital for Women and Newborns — San Diego, California, United States

Full record on ClinicalTrials.gov

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