Skip to main content
Clinical Trials/NCT02708862
NCT02708862
Completed
Not Applicable

Comparison of Emergency Department Preoxygenation Techniques in Healthy Volunteers

Hennepin Healthcare Research Institute0 sites26 target enrollmentMarch 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Respiratory Failure
Sponsor
Hennepin Healthcare Research Institute
Enrollment
26
Primary Endpoint
Exhaled Oxygen Concentration
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Four methods of preoxygenation will be compared in healthy volunteers

Detailed Description

After informed consent, each volunteer will undergo the following techniques: Simple mask at "flush" flow (40-60 L/min) Non-rebreather mask at 15 L/min Non-rebreather mask at 60 L/min Bag valve mask with one way exhalation valve at 15 L/min After 3 minutes, the exhaled oxygen will be measured with an oxygen sensor

Registry
clinicaltrials.gov
Start Date
March 2016
End Date
March 2016
Last Updated
6 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Brian Driver

Associate Research Director

Hennepin Healthcare Research Institute

Eligibility Criteria

Inclusion Criteria

  • Over 18 years old

Exclusion Criteria

  • Any active respiratory pathology (asthma, chronic obstructive pulmonary disease, other lung disease, smoking history more than 5 years)

Outcomes

Primary Outcomes

Exhaled Oxygen Concentration

Time Frame: Immediately after 3 minutes of oxygen supplementation

Subjects will blow into an oxygen sensor after each method (arm). The primary outcome will be a non-inferiority test between bag valve mask and non-rebreather at 60 L/min. The remaining tests will be completed for comparison, but not part of formal statistical testing.

Similar Trials