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Apneic Oxygenation Including Precipitous Intubations During RSI in the ED

Randomized Controlled Trial of Apneic Oxygenation Including Precipitous Intubations During RSI in the Emergency Department

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03694379
Acronym
RAPID
Enrollment
10
Registered
2018-10-03
Start date
2019-03-01
Completion date
2020-03-22
Last updated
2020-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Apneic Oxygenation, Endotracheal Intubation

Keywords

Apneic Oxygenation, Endotracheal intubation, Airway Management, Emergency Department

Brief summary

This RCT is testing the efficacy of apneic oxygenation during endotracheal intubation in the emergency department. Currently the standard practice in the ED when performing endotracheal intubation is that some providers use apneic oxygenation (the application of a nasal cannula at 15LPM) throughout the intubation procedure, while others do not apply apneic oxygenation. Initial literature in the operating room showed that apneic oxygenation helps prevent desaturation during the procedure. However, the latest literature conducted in critical care settings (one study in the ICU and one in the ED) questions the efficacy of this intervention in critically ill patients; however, no harm has been shown. Our study aims to test this intervention further by adding in a special subset of patients that was excluded from prior studies, precipitous intubations, or those patients that have to be intubated quickly and cannot have adequate pre-oxygenation. We hypothesize that apneic oxygenation will be more efficacious in this subset than in the overall ED population. We will randomize patients requiring endotracheal intubation into intervention (apneic oxygenation) and control (no apneic oxygenation). We will measure the lowest arterial oxygen saturation from the start of the intubation procedure through 2 minutes after intubation is complete.

Interventions

OTHERApneic oxygenation during endotracheal intubation

Providing oxygenation through nasal cannula during the apneic phase of endotracheal intubation.

Sponsors

Rutgers, The State University of New Jersey
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* The inclusion criteria for our study will include patients 18 years or older who require emergent endotracheal intubation utilizing rapid sequence intubation (RSI) in the Emergency Department with first attempt taken by a resident or attending physician working in the emergency department. This includes Emergency Medicine attending physicians and residents as well as non-Emergency Medicine rotators (e.g.., Internal Medicine residents who are rotating through the Emergency Department).

Exclusion criteria

*

Design outcomes

Primary

MeasureTime frameDescription
Lowest oxygen saturation overallTime between neuromuscular blockade and 2 minutes after completion of endotracheal intubationLowest oxygen saturation between overall control and intervention groups

Secondary

MeasureTime frameDescription
Need for additional intubating equipmentFrom first attempt at intubation through completion of endotracheal intubation procedure, approximately 2 minutes.The operator needed to change or add equipment to facilitate intubation
Lowest oxygen saturation precipitous intubationsTime between neuromuscular blockade and 2 minutes after completion of endotracheal intubationLowest oxygen saturation between control and intervention groups that did not receive adequate pre-oxygenation only
Lowest oxygen saturation pre-oxygenationTime between neuromuscular blockade and 2 minutes after completion of endotracheal intubationLowest oxygen saturation between control and intervention groups that did receive
Difference in baseline and final oxygen saturationDecision to intubate through 2 minutes after completion of endotracheal intubation
Difference in oxygen saturation before and after apneic periodInitiation of neuromuscular blockade through 2 minutes after completion of endotracheal intubation
DesaturationInitiation of neuromuscular blockade through 2 minutes after completion of endotracheal intubationThe proportion of patients who desaturate below 90%
Esophageal intubationsFrom first attempt at intubation through entire ED stay, approximately 6 hours.The proportion of intubations that resulted in the endotracheal tube being placed in the esophagus
Need for second operatorFrom first attempt at intubation through completion of endotracheal intubation procedure, approximately 2 minutes.A second physician had to attempt intubation
Procedural hypotensionInitiation of neuromuscular blockade to 2 minutes after completion of endotracheal intubationProportion of became hypotensive at any point during the intubation procedure
AspirationWithin 24 hours after intubation procedure was completeProportion of patients that had evidence of aspiration
Hospital length of stayUp to 28 days after intubationNumber of days patient is hospitalized
Number of days intubatedUp to 28 days after intubation
In-hospital mortalityUp to 28 days after intubation
number of attemptsFrom first attempt at intubation through completion of endotracheal intubation procedure, approximately 2 minutes.number of times laryngoscope is placed into the mouth in an attempt to pass an endotracheal tube

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026