Trials / Completed
CompletedNCT02828280
NuMask Versus Traditional Mask Ventilation During Routine Care
A Comparison of Controlled Ventilation With the NuMask vs. Traditional Mask Ventilation.
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 44 (actual)
- Sponsor
- Derek Sakata · Academic / Other
- Sex
- All
- Age
- 18 Years – 64 Years
- Healthy volunteers
- Accepted
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
Interventions
| Type | Name | Description |
|---|---|---|
| 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 |
Timeline
- Start date
- 2011-05-01
- Primary completion
- 2014-01-01
- Completion
- 2014-01-01
- First posted
- 2016-07-11
- Last updated
- 2017-05-09
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT02828280. Inclusion in this directory is not an endorsement.