NCT01223274View on ClinicalTrials.gov

Delivery Room CPAP in Extremely Low Birth Weight Infants

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

104

Participants

Timeline

Start Date

July 31, 2002

Primary Completion Date

January 31, 2003

Study Completion Date

January 31, 2003

Conditions
Infant, NewbornInfant, Low Birth WeightInfant, Small for Gestational AgeInfant, PrematureBronchopulmonary DysplasiaContinuous Positive Airway Pressure
Interventions
DEVICE

CPAP/PEEP

Infants received 100% oxygen by facemask and continuous positive airway pressure (CPAP) or positive pressure ventilation (PPV) with positive end-expiratory pressure (PEEP), if the infant required PPV.

DEVICE

Standard management practices

Control infants were treated with 100% oxygen and no CPAP. When a control infant required PPV, no PEEP was used.

Trial Locations (6)

27705

RTI International, Durham

33136

University of Miami, Miami

35233

University of Alabama at Birmingham, Birmingham

44106

Case Western Reserve University, Rainbow Babies and Children's Hospital, Cleveland

45267

Cincinnati Children's Medical Center, Cincinnati

92103-8774

University of California at San Diego, San Diego

All Listed Sponsors
collaborator

National Center for Research Resources (NCRR)

NIH

lead

NICHD Neonatal Research Network

NETWORK

NCT01223274 - Delivery Room CPAP in Extremely Low Birth Weight Infants | Biotech Hunter | Biotech Hunter