Follow-up at School-age of Children Who Participated in the Efficacy Study of Nitric Oxide for Premature Infants

PHASE3CompletedINTERVENTIONAL
Enrollment

160

Participants

Timeline

Start Date

May 31, 2005

Primary Completion Date

September 30, 2006

Study Completion Date

September 30, 2006

Conditions
Prematurity, Respiratory Distress Syndrome,Hypoxemia
Interventions
DRUG

Inhaled nitric oxide

1 day of iNO at 10 ppm, then 5 ppm of iNO for days 2-7

DRUG

Placebo

No iNO given for days 1-7

Trial Locations (1)

60637

The University of Chicago, Comer Children's Hospital,, Chicago

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Mallinckrodt

INDUSTRY

lead

University of Chicago

OTHER