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NCT03694379 · ClinicalTrials.gov registry record · NA
Apneic Oxygenation Including Precipitous Intubations During RSI in the ED
A NA study, sponsored by Rutgers, The State University of New Jersey.
- Terminated
- Registry status
- NA
- Development phase
- 10
- Enrollment target
NCT03694379 is a NA study that was terminated before completion, run by Rutgers, The State University of New Jersey. The registered enrollment target is 10 participants.
The verdict
NCT03694379, a NA study, was terminated before completion, sponsored by Rutgers, The State University of New Jersey.
- TERMINATED
- Registry status
- NA
- Development phase
- 10 participants
- Enrollment target
Study 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
- OTHER Apneic oxygenation during endotracheal intubation
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2019-03-01 |
| Est. Completion | 2020-03-22 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03694379
The ClinicalTrials.gov registry entry for NCT03694379 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rutgers, The State University of New Jersey, which has 413 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Apneic oxygenation during endotracheal intubation is the first listed.
NCT03694379 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03694379 about?
NCT03694379 is a clinical study titled "Apneic Oxygenation Including Precipitous Intubations During RSI in the ED". 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 ...
What is the current status of trial NCT03694379?
This trial is currently terminated. It is a NA study. The enrollment target is 10 participants. The study started on 2019-03-01. Estimated completion is 2020-03-22.
What interventions are being tested in trial NCT03694379?
The interventions under investigation include: Apneic oxygenation during endotracheal intubation (OTHER).
Who is sponsoring clinical trial NCT03694379?
This trial is sponsored by Rutgers, The State University of New Jersey, which has 413 total clinical trials registered on ClinicalTrials.gov.
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