Clinical trial

Treatment of Delayed Pulmonary Transition in Extremely Preterm Infants & Bronchopulmonary Dysplasia

Name
1170748
Description
Inhaled nitric oxide (iNO) is an effective treatment for pulmonary hypertension (PH) in term and near-term infants. Preterm infants are at risk for early PH that is associated with high risk for bronchopulmonary dysplasia or death. In multiple clinical trials, iNO treatment was not effective for BPD prevention. However, infants were not screened for PH and iNO treatment was not targeted for PH. iNO treatment for PH in preterm infants is controversial due to lack of evidence. The study team hypothesizes that early diagnosis of PH (72-96 hours of life) and iNO treatment will decrease the incidence of death and bronchopulmonary dysplasia and improve oxygenation in extremely preterm infants. 1. To determine if iNO treatment of extremely preterm infants with early pulmonary hypertension as established with echocardiographic evidence at 72-96 hours of age will decrease incidence of death or BPD. 2. To determine if iNO treatment of extremely preterm infants with early PH will decrease the pulmonary artery pressure and improve oxygenation within 72 hours of intervention.
Trial arms
Trial start
2019-07-15
Estimated PCD
2024-12-01
Trial end
2024-12-01
Status
Recruiting
Phase
Early phase I
Treatment
inhaled nitric oxide
inhaled nitric oxide will be administered starting at 20 ppm. Treatment will continue for 14 days or until resolution of pulmonary hypertension
Arms:
Treatment group - active
Other names:
iNO
Placebo
placebo will be administered starting at 20 ppm. Treatment will continue for 14 days or until resolution of pulmonary hypertension
Arms:
Treatment group - placebo
Size
138
Primary endpoint
Death (yes/no)
36 weeks post menstrual age
Bronchopulmonary (BPD) dysplasia (yes/no)
36 weeks post menstrual age
Eligibility criteria
Inclusion Criteria: Step 1: * Birth between 23 weeks and 0 days and 29 weeks and 6 days. * Positive pressure ventilation at 72-96 hours of age Step 2: * Early pulmonary hypertension Exclusion Criteria: Step 1: * Death prior to 12 hours of age or first echocardiogram * Chromosomal anomalies * Major congenital anomalies * Myocardial dysfunction * Complex cardiac defect * Dependent on right to left shunting of blood Step 2: * Excessive pulmonary blood flow (left to right shunt across PDA) * Pulmonary blood flow obstruction secondary to pulmonary vein stenosis * Mitral valve stenosis * Cor triata * Aortic valve atresia
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE1', 'PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'Masked randomized controlled trial', 'primaryPurpose': 'PREVENTION', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 138, 'type': 'ESTIMATED'}}
Updated at
2023-06-29

1 organization

1 product

1 drug

2 indications

Organization
AdventHealth