Delivery Room Practice Change Following the Initiation of the NICHD SUPPORT Trial

Completed

Conditions studied: Preterm Birth

In brief

This study was designed to analyze whether initiation of the NICHD Neonatal Research Network SUPPORT trial was followed by a change in frequency of endotracheal intubation the delivery room in non-participants and whether these changes were associated with changes in management and outcomes. The investigators hypothesized that the investigators would observe following the initiation of the SUPPORT trial a 33% reduction in the rate of intubation in the delivery room among non-participants preterm infants at Parkland Memorial Hospital.

Key facts

Study ID

NCT01601886

Run by

Luc Brion

People needed

3843

Starts

2008-04-01

Expected to finish

2012-04-01

Last updated by the study team

2012-05-18

Who can join

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

You may qualify if…

• All babies born at Parkland Memorial Hospital with gestational age at least 24 weeks and less than 35 weeks between 01/2003 and 06/2010

You may not qualify if…

• Infants receiving comfort care
• Those with major congenital anomalies
• Those enrolled in the SUPPORT trial

Where it is running

• University of Texas Southwestern — Dallas, Texas, United States

Full record on ClinicalTrials.gov

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