Delivery Room Management Trial of Premature Infants at High Risk of Respiratory Distress Syndrome

PHASE3CompletedINTERVENTIONAL
Enrollment

648

Participants

Timeline

Start Date

August 31, 2003

Primary Completion Date

June 30, 2009

Study Completion Date

June 30, 2011

Conditions
Respiratory Distress Syndrome, Newborn
Interventions
DRUG

PS Group

Intubation, prophylactic surfactant administration shortly after delivery, and subsequent stabilization on ventilator support.

DEVICE

NCPAP Group

Early stabilization on nasal continuous positive airway pressure (NCPAP) with selected intubation and surfactant administration for clinical indications.

DRUG

ISX Group

Intubation, prophylactic surfactant administration shortly after delivery, and rapid extubation to nasal CPAP.

Trial Locations (1)

05401

Vermont Oxford Network, Burlington

All Listed Sponsors
lead

Vermont Oxford Network

NETWORK

NCT00244101 - Delivery Room Management Trial of Premature Infants at High Risk of Respiratory Distress Syndrome | Biotech Hunter | Biotech Hunter