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Clinical Trial Summary

The purpose of the study is to randomly and prospectively evaluate the differences in outcomes between the control group (closed full facemask immediate post-extubation with standard oxygenating device used post-operatively in PACU) and the SuperNO2VA™ group (SuperNO2VA™ immediate post-extubation and post-operatively in PACU)


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03969615
Study type Interventional
Source Vyaire Medical
Contact Carin Hagberg, MD
Phone 7135633511
Email chagberg@mdanderson.org
Status Recruiting
Phase N/A
Start date October 15, 2018
Completion date October 15, 2019

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