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Clinical Trial Summary

The direct objective of this study is to determine whether an experienced provider can more adequately and/or easily ventilate an anesthetized patient with the NuMask device as compared to traditional bag-valve-mask ventilation. These are approved masks, being used in the patients routine care. The researchers believe that mean tidal volumes obtained by experienced providers when manually ventilating anesthetized patients with the NuMask device will be larger than when using the traditional bag-valve-mask.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02828280
Study type Observational
Source University of Utah
Contact
Status Completed
Phase N/A
Start date May 2011
Completion date January 2014

See also
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