Utah Study Evaluating Apneic Oxygenation for Emergency Department Intubation

N/AUnknownNCT02961933

Intermountain Health Care, Inc.500 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

500

Conditions

Intubation

Interventions

Apneic oxygenationOTHER

Nasal cannula apneic oxygenation

Pre-oxgenation with NRB, NIPPV, BVMOTHER

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

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: \- Patients requiring emergent Rapid Sequence or Delayed Sequence endotracheal intubation with administration of a neuromuscular blocker (Succinylcholine, Rocuronium) Exclusion Criteria: * Known prisoners * Patients in cardiac arrest * Patients who are intubated without the use of neuromuscular blockade (i.e., cardiac arrest, awake intubation).

Locations (1)

Intermountain Medical Center

Murray, Utah, United States

RECRUITING

Outcomes

Primary Outcomes

First pass success without hypoxemia

Time frame: 10 minutes

Secondary Outcomes

Change in peri-intubation saturation

Time frame: 0, 30, 60 and 120 seconds

Saturation at time of tube placement

Time frame: 10 minutes

Time to desaturation <93%

Time frame: measured time until saturations drop below 93% during the peri-intubation period, up to 10 minutes

Saturation at post intubation

Time frame: 0, 30, 60, and 120 seconds

Central Contacts

Valerie Aston, MBA, RT

CONTACT

801-507-4606 valerie.aston@imail.org

Data from ClinicalTrials.gov

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