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Clinical Trial Summary

This study is to evaluate the feasibility of using a pressure limited nasal cannula system instead of a high flow nasal cannula system in the management of premature babies with respiratory distress.


Clinical Trial Description

NCPAP has been used increasingly to manage respiratory distress in newborns as well as apnea of prematurity. Humidified high flow nasal cannula devices (flows 1-8 lpm) have also been used in neonatal intensive care units. This study is to evaluate the feasibility of using a pressure limited nasal cannula system instead of a high flow nasal cannula system in the management of premature babies with respiratory distress. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03171129
Study type Interventional
Source Loma Linda University
Contact Tina Ramirez
Phone 909-558-5828
Email TIRameriz@llu.edu
Status Not yet recruiting
Phase N/A
Start date September 2024
Completion date September 2025