Inhaled Nitric Oxide for Preventing Chronic Lung Disease in Premature Infants
Lung Diseases, Bronchopulmonary Dysplasia
About this trial
This is an interventional prevention trial for Lung Diseases
Eligibility Criteria
Inclusion Criteria: Weighing between 500 to 1250 grams at birth Gestational age of less than 34 weeks Less than 48 hours old Respiratory failure on mechanical ventilation Absence of structural heart disease (PDA, ASD less than 1 cm, or VSD less than 2 mm are permitted if known prior to study entry) Absence of lethal congenital anomaly Exclusion Criteria: Concurrent participation in another experimental study (observational studies will be allowed with prior approval by the Steering Committee and Data and Safety Monitoring Board) Active pulmonary hemorrhage Unevaluated pneumothorax High frequency jet ventilation Expected short duration of ventilation (less than 48 hours from birth)
Sites / Locations
- St. Joseph's Hospital
- Loma Linda University Medical Center
- Univeristy of Southern California/Good Samaritan Hospital
- Children's Hospital
- University of Connecticut Health Center
- University of Iowa Hospital & Clinics
- University of North Carolina Chapel Hill
- Duke University Medical Center
- Children's Hospital of Oklahoma
- Pennsylvania Hospital
- Magee-Women's Hospital
- Medical University of South Carolina
- Vanderbilt University Medical Center
- Utah Valley Regional Medical Center
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Inhaled Nitric Oxide (iNO)
Placebo
Nitric Oxide study gas will be initiated at 5 ppm using the INOvent delivery system. The delivery system provides for masked delivery of the treatment gas. This dose will be used for a 21-day period or until extubation.