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Salt Lake City, Utah 84132


This study will seek to enroll neonates requiring Nasal Continuous Airway Pressure (NCPAP) respiratory support and randomize them to either oscillatory (Osc-NCPAP, study group) or non-oscillatory (NCPAP, control group) mode. The goal of the research is to determine if Osc-NCPAP provides improved ventilation support compared to routine NCPAP, i.e. NCPAP without oscillations. This will be measured by need for change to ventilator support, improvement in pCO2 values, and reduction in respiratory rate and frequency of apnea during the period of NCPAP treatment. Other respiratory outcomes will also be compared, including time on NCPAP, time on High-Flow Nasal Cannula support following NCPAP, and time-averaged PiO2 from start of study to end of respiratory treatment.


Inclusion Criteria: - Newborn (0-28 days of age) admitted to Neonatal Intensive Care Unit (NICU) - Ordered respiratory treatment of NCPAP Exclusion Criteria: - Major congenital defect - Known or suspected chromosomal disorder



Primary Contact:

Principal Investigator
Donald Null, MD
University of Utah

Backup Contact:


Location Contact:

Salt Lake City, Utah 84132
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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