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Clinical Trial Summary

The primary aim of this study is to quantify and compare changes in lung volumes (as measured by functional residual capacity) in premature infants stable on continuous positive airway pressure (CPAP), and then randomized to two additional weeks of CPAP and room air versus room air alone. We hypothesize that infants randomized to additional CPAP will demonstrate an increased functional residual capacity (at the end of the two week study period and prior to discharge) compared to those randomized to room air.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02249143
Study type Interventional
Source Oregon Health and Science University
Contact
Status Completed
Phase N/A
Start date September 2014
Completion date September 2017

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