EmergeNcy Department Apneic Oxygenation Versus Usual Care During Rapid Sequence Intubation
Diffuse Apneic Oxygenation
Bottom Line
View on ClinicalTrials.gov: NCT02737917 ↗Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Oxygen (Other); Standard of care (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- New York City Health and Hospitals Corporation
- Primary completion
- Dec 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Mean (Average) Arterial Oxygen Saturation |
92; 93 | — |
| SECONDARY Rates of Desaturation |
17; 15; 3; 4; 80; 81 | — |
Summary
Eligibility Criteria
Inclusion Criteria
Any patient greater than 18 years of age that presents to the Lincoln medical and Mental Health Center Emergency Department requiring endotracheal intubation.
Exclusion Criteria
Patients will be excluded from the primary outcome analysis, but included in the intention to treat analysis for the secondary outcome if they are not pre-oxygenated to the standard RSI protocol of 3 minutes with 100% fraction of inspired oxygen (FiO2) by means of bag valve mask, HFNC and/or non-rebreather; patients will be excluded from the study in general if they are in cardiac or traumatic arrest or they are intubated without an apneic period (awake intubation)
Data sourced from ClinicalTrials.gov (NCT02737917). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.