Utah Study Evaluating Apneic Oxygenation for Emergency Department Intubation
Not Applicable
- Conditions
- Intubation
- Interventions
- Other: Apneic oxygenationOther: Pre-oxgenation with NRB, NIPPV, BVM
- Registration Number
- NCT02961933
- Lead Sponsor
- Intermountain Health Care, Inc.
- Brief 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 500
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).
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Apneic oxygenation Apneic oxygenation - non-apneic oxygenation Pre-oxgenation with NRB, NIPPV, BVM -
- Primary Outcome Measures
Name Time Method First pass success without hypoxemia 10 minutes
- Secondary Outcome Measures
Name Time Method Change in peri-intubation saturation 0, 30, 60 and 120 seconds Saturation at time of tube placement 10 minutes Time to desaturation <93% measured time until saturations drop below 93% during the peri-intubation period, up to 10 minutes Saturation at post intubation 0, 30, 60, and 120 seconds
Trial Locations
- Locations (1)
Intermountain Medical Center
🇺🇸Murray, Utah, United States