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NCT07869719
nCPAP Versus High-Flow Nasal Cannula in Preterm Infants With RDS
Conditions: Respiratory Distress Syndrome, Premature Birth
Sex: All
Ages: N/A – 28 Days
Healthy volunteers: No
Phase: NA
Enrollment: 94
Sponsor: Assiut University
Summary
This randomized controlled trial aims to compare the efficacy and safety of nasal continuous positive airway pressure versus high-flow nasal cannula as initial non-invasive respiratory support in preterm infants with respiratory distress syndrome.
Eligibility Criteria
Inclusion Criteria:
* \- Preterm infants with gestational age 28 to 36 weeks and 6 days
* Clinical diagnosis of respiratory distress syndrome
* Spontaneous breathing without immediate need for invasive mechanical ventilation
* Requirement for non-invasive respiratory support
* Written informed consent from parent or legal guardian
Exclusion Criteria:
* \- Infants requiring immediate endotracheal intubation and mechanical ventilation
* Major congenital anomalies affecting the respiratory or cardiovascular systems
* Congenital diaphragmatic hernia
* Significant congenital heart disease
* Severe perinatal asphyxia requiring prolonged resuscitation
* Severe hemodynamic instability
* Prolonged mechanical ventilation before enrollment
Source: ClinicalTrials.gov (NCT07869719). StuddyBuddy aggregates publicly available trial information.