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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: Completed NA study, sponsored by Vanderbilt University Medical Center.

NCT05239195 is a NA study that has completed, run by Vanderbilt University Medical Center. The registered enrollment target is 1,420 participants, roughly in line with the 1,404-participant average among 58,714 other NA trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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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.

Primary Outcome

The primary outcome is defined as placement of an endotracheal tube in the trachea with a single insertion of a laryngoscope blade into the mouth and EITHER a single insertion of an endotracheal tube into the mouth OR a single insertion of a bougie into the mouth followed by a single insertion of an endotracheal tube over the bougie into the mouth.

Interventions

  • OTHER Video Laryngoscope
  • OTHER Direct Laryngoscope

Trial Details

FieldValue
Enrollment Target 1,420 participants
Start Date 2022-03-19
Est. Completion 2022-12-16
Phase NA

What the finished NCT05239195 record still lists

NCT05239195 is an interventional study that assigns participants to a tested intervention. Its 1,420 participants enrollment target places it among the larger protocols in the corpus, roughly in line with the 1,404-participant average among 58,714 other NA trials with a reported enrollment target.

The record links to 0 conditions, and to 2 interventions - of which Video Laryngoscope is the first listed.

NCT05239195 does not publish any study locations in the registry export this page uses.

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.

How this trial's enrollment target compares

Where NCT05239195's enrollment target sits among peer trials

1,420 70th of 2000 higher than 1,931 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05239195, the US trial registry maintained by the National Library of Medicine. NCT05239195 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.