Oscillatory Versus Non-Oscillatory Nasal Continuous Airway Pressure Neonatal Respiratory Support



Status:Suspended
Conditions:Hospital, Pulmonary
Therapuetic Areas:Pulmonary / Respiratory Diseases, Other
Healthy:No
Age Range:Any
Updated:4/21/2016
Start Date:December 2014
End Date:January 2017

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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
We found this trial at
3
sites
100 N Mario Capecchi Dr
Salt Lake City, Utah 84132
(801) 662-1000
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Salt Lake City, UT
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Madera, California 93636
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Madera, CA
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Salt Lake City, Utah 84132
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Salt Lake City, UT
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