Neonatal Respiratory Distress Clinical Trial
Official title:
A Comparative Study Between Postextubation of Preterm Infants Into High-Flow Nasal Cannulae V.S Nasal Continuous Positive Airway Pressure
The investigators hypothesize that there is a growing trend of the feasibility of HFNC as an alternative to other forms of non-invasive ventilation mechanism to provide continuous distending pressure to preterm infants. However, there remains uncertainty about the efficacy and safety of HFNC in this population.
Our primary outcome is to determine whether postextubation respiratory support via heated
humidified high-flow nasal cannula results in a greater proportion of infants younger than 34
weeks gestation being successfully extubated after a period of endotracheal positive pressure
ventilation compared with conventional (NCPAP).
The following study will be conducted in the neonatal intensive care unit (NICU) of
Gynecology and Obstetric department of Kasr El Aini hospital and neonatal intensive care unit
of Military Hospital throughout a time interval of at least 6 months for a minimum of 100
preterm infants.
Infants will be eligible for the study if they born at less than 34 weeks' gestation,
required endotracheal intubation and positive pressure ventilation, and considered ready for
extubation by the clinical team.
The investigators will assign extubation of preterm ventilated infants (50 preterm infant) in
NICU of Military Hospital into HHFNC and extubation of preterm ventilated infants (50 preterm
infant) in (NICU) of Gynecology and Obstetric department of Kasr El Aini hospital into NCPAP
(50 preterm infant).
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