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NuMask Versus Traditional Mask Ventilation During Routine Care

NCT02828280 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 44

Last updated 2017-05-09

No results posted yet for this study

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.

Conditions

  • Apnea

Interventions

DEVICE

NuMask

The NuMask is a relatively new mask ventilation device that has been registered with the FDA and used in the United States since 2006.

DEVICE

Traditional mask

A traditional air inflated facemark used to ventilate patients

Sponsors & Collaborators

  • Derek Sakata

    lead OTHER

Principal Investigators

  • Derek Sakata, MD · University of Utah

Eligibility

Min Age
18 Years
Max Age
64 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2014-01-31
Completion
2014-01-31
FDA Device
Yes

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02828280 on ClinicalTrials.gov