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NCT05239195 · ClinicalTrials.gov registry record · NA
DirEct Versus VIdeo LaryngosCopE Trial
A NA study, sponsored by Vanderbilt University Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 1,420
- Enrollment target
NCT05239195 is a NA study that has completed, run by Vanderbilt University Medical Center. The registered enrollment target is 1,420 participants.
The verdict
NCT05239195, a NA study, has completed, sponsored by Vanderbilt University Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 1,420 participants
- Enrollment target
Study Summary
Clinicians perform rapid sequence induction, laryngoscopy, and tracheal intubation for more than 5 million critically ill adults as a part of clinical care each year in the United States. Failure to intubate the trachea on the first attempt occurs in more than 10% of all tracheal intubation procedures performed in the emergency department (ED) and intensive care unit (ICU). Improving clinicians rate of intubation on the first attempt could reduce the risk of serious procedural complications. In current clinical practice, two classes of laryngoscopes are commonly used to help clinicians view the larynx while intubating the trachea: a video laryngoscope (equipped with a camera and a video screen) and a direct laryngoscope (not equipped with a camera or video screen). For nearly all laryngoscopy and intubation procedures performed in current clinical practice, clinicians use either a video or a direct laryngoscope. Prior research has shown that use of a video laryngoscope improves the operator's view of the larynx compared to a direct laryngoscope. Whether use of a video laryngoscope increases the likelihood of successful intubation on the first attempt remains uncertain. A better understanding of the comparative effectiveness of these two common, standard-of-care approaches to laryngoscopy and intubation could improve the care clinicians deliver and patient outcomes.
Interventions
- OTHER Video Laryngoscope
- OTHER Direct Laryngoscope
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,420 participants |
| Start Date | 2022-03-19 |
| Est. Completion | 2022-12-16 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05239195
The ClinicalTrials.gov registry entry for NCT05239195 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 1,420 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanderbilt University Medical Center, which has 677 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Video Laryngoscope is the first listed.
NCT05239195 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT05239195 about?
NCT05239195 is a clinical study titled "DirEct Versus VIdeo LaryngosCopE Trial". Clinicians perform rapid sequence induction, laryngoscopy, and tracheal intubation for more than 5 million critically ill adults as a part of clinical care each year in the United States. Failure to intubate the trachea on the first attempt occurs in more than 10% of all tracheal intubation procedur...
What is the current status of trial NCT05239195?
This trial is currently completed. It is a NA study. The enrollment target is 1,420 participants. The study started on 2022-03-19. Estimated completion is 2022-12-16.
What interventions are being tested in trial NCT05239195?
The interventions under investigation include: Video Laryngoscope (OTHER), Direct Laryngoscope (OTHER).
Who is sponsoring clinical trial NCT05239195?
This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.
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