RecruitingPhase 4NCT06007547
Prophylactic Minimally Invasive Surfactant Evaluation
Sponsor
Endeavor Health
Enrollment
200 participants
Start Date
Jan 1, 2024
Study Type
INTERVENTIONAL
Conditions
Summary
The purpose of this study is to explore the question: Does prophylactic administration of exogenous surfactant in the delivery room, using a minimally-invasive technique, improve outcome in preterm infants 22-29 weeks' gestation compared to rescue treatment using the same technique?
Eligibility
Max Age: 15 Minutes
Inclusion Criteria2
- Gestational age <30 weeks
- Antenatal consent from Parent
Exclusion Criteria2
- Congenital anomalies
- Alternate cause of respiratory distress
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Interventions
DRUGPoractant Alfa
Poractant alfa (Curosurf) 200mg/kg administered under direct laryngoscopy using a surfactant instillation catheter
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06007547
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