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Utah Study Evaluating Apneic Oxygenation for Emergency Department Intubation

NCT02961933 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 500

Last updated 2020-02-11

No results posted yet for this study

Summary

This study will determine rates of first pass success without hypoxemia in emergency department intubations with and without the use of apneic oxygenation by nasal cannula.

Conditions

  • Intubation

Interventions

OTHER

Apneic oxygenation

Nasal cannula apneic oxygenation

OTHER

Pre-oxgenation with NRB, NIPPV, BVM

Pre-oxygenation with non-rebreather mask, non-invasive positive pressure ventilation, or bag-valve mask

Sponsors & Collaborators

Principal Investigators

  • Robert Bryant, MD · Intermountain Health Care, Inc.

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-12-31
Primary Completion
2020-01-31
Completion
2020-06-30

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT02961933 on ClinicalTrials.gov