Utah Study Evaluating Apneic Oxygenation for Emergency Department Intubation
NCT ID: NCT02961933
Last Updated: 2020-02-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
500 participants
INTERVENTIONAL
2016-12-31
2020-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Apneic oxygenation
Apneic oxygenation
Nasal cannula apneic oxygenation
non-apneic oxygenation
Pre-oxgenation with NRB, NIPPV, BVM
Pre-oxygenation with non-rebreather mask, non-invasive positive pressure ventilation, or bag-valve mask
Interventions
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Apneic oxygenation
Nasal cannula apneic oxygenation
Pre-oxgenation with NRB, NIPPV, BVM
Pre-oxygenation with non-rebreather mask, non-invasive positive pressure ventilation, or bag-valve mask
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Patients in cardiac arrest
* Patients who are intubated without the use of neuromuscular blockade (i.e., cardiac arrest, awake intubation).
18 Years
ALL
No
Sponsors
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University of Utah
OTHER
Intermountain Health Care, Inc.
OTHER
Responsible Party
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Principal Investigators
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Robert Bryant, MD
Role: PRINCIPAL_INVESTIGATOR
Intermountain Health Care, Inc.
Locations
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Intermountain Medical Center
Murray, Utah, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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1050200
Identifier Type: -
Identifier Source: org_study_id
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