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

NCT01601886 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3843

Last updated 2012-05-18

No results posted yet for this study

Summary

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.

Conditions

Sponsors & Collaborators

  • University of Texas Southwestern Medical Center

    collaborator OTHER
  • Luc Brion

    lead OTHER

Principal Investigators

  • Luc P Brion, MD · University of Texas

Eligibility

Min Age
24 Weeks
Max Age
35 Weeks
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-04-30
Primary Completion
2011-11-30
Completion
2012-04-30

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01601886 on ClinicalTrials.gov