Phase 3
Completed N=800
Safety and Efficacy Study of Nitric Oxide for Inhalation on Chronic Lung Disease in Premature Babies
Source: ClinicalTrials.gov NCT00551642 ↗Enrolled (actual)
800
Serious AEs
43.8%
Results posted
Oct 2010
Primary outcomePrimary: Survival Without Bronchopulmonary Dysplasia (BPD) in Preterm Infants With Respiratory Distress — 258; 262 Participants — p=0.7340
Summary
The purpose of this study is to assess the safety and efficacy of inhaled nitric oxide to reduce the risk of chronic lung disease in pre-term infants with respiratory distress, and to assess the long-term effects of the therapy on the development of these children over 7 years of clinical follow-up.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Survival Without Bronchopulmonary Dysplasia (BPD) in Preterm Infants With Respiratory Distress |
258; 262 | 0.7340 |
Eligibility Criteria
Inclusion Criteria
- Inborn preterm infants 24+0 weeks-28+6 days weeks gestational age (defined by first trimester ultrasound or if not available based on the last menstrual period) who requires the use of surfactant within 24 hours of birth (either prophylactically, or for signs of developing respiratory distress), or who requires the use of continuous positive airway pressure (CPAP) (fraction of inspired oxygen concentration (FiO2) ≥ 0.30 on a mean airway pressure ≥ 4cm water (H2O)) within 24 hours of birth in order to maintain an oxygen saturation (SpO2) ≥ 85%.
- Informed consent of the guardian.
Exclusion Criteria
- Outborn infants.
- Infants ≥ 29 weeks gestational age.
- Infants requiring FiO2 >0.5 to maintain SpO2 >85%, on a sufficient mean airway pressure (e.g., > 8 cm H2O on controlled mechanical ventilation (CMV)) in order to achieve adequate chest inflation (8-9 ribs on Chest X-ray) two hours after the proper administration of exogenous surfactant.
- Any suspected congenital heart disease other than patent ductus arteriosus or atrial septal defect.
- Any infant with severe bleeding or coagulation abnormalities at high-risk of diathesis, e.g., platelet <50,000 per millimeter cube (mm³), fibrinogen <0.5 gram per liter (g/L), other clotting factors <10%.
- Any infant in whom a decision has been made not to provide full treatment, e.g., chromosomal abnormalities, severe multiple abnormalities, severe birth asphyxia, etc.
- Use of another investigational drug or device before or during the active study period.
Data sourced from ClinicalTrials.gov (NCT00551642). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.