Clinical Trial

High-Flow Nasal Cannula Versus Nasal CPAP as Primary Support in Preterm Respiratory Distress Syndrome

Completed
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Summary
This single-center randomized controlled trial compared heated humidified high-flow nasal cannula (HHHFNC) with nasal continuous positive airway pressure (nCPAP) as primary noninvasive respiratory support in preterm infants (gestational age 28-34 weeks; birth weight 1000-2000 g) with moderate respiratory distress syndrome. The primary outcome was treatment failure requiring invasive mechanical ventilation within the first 7 days.
Trial Details
NCT Number NCT07693530
Lead Sponsor Kayseri City Hospital
Conditions Premature Birth, Respiratory Distress Syndrome, Newborn
Enrollment 86 participants
Start Date 2020-06-01
Primary Completion 2022-05-01 (estimated)
Study Completion 2022-05-01 (estimated)
Updated on ClinicalTrials.gov 2026-07-09