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Conventional vs. Video-Assisted Laryngoscopy for Perioperative Endotracheal Intubation — COVALENT  

Endotracheal Intubation Clinical Trial

Official title:
Conventional vs. Video-Assisted Laryngoscopy for Perioperative Endotracheal Intubation

Clinical Trial Summary

COVALENT is a randomized, controlled, multi-center study that aims to evaluate the clinical routine practice of endotracheal intubation in an operative setting comparing video-assisted laryngoscopy to direct laryngoscopy.

Clinical Trial Description

Data on the routine use of video-assisted laryngoscopy in peri-operative intubations are rather inconsistent and ambiguous, in part due to small study populations and non-uniform outcome measures in past trials. Failed or prolonged intubation procedures are a reason for relevant morbidity and mortality. This study aims to determine whether video-assisted laryngoscopy (irrespective of the shape of the blade) is non-inferior to the standard method of direct laryngoscopy with respect to the first-pass success rate. Furthermore, validated tools from the field of human factors will be applied to examine within-team communication and task load during this critical medical procedure. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05228288
Study type Interventional
Source Wuerzburg University Hospital
Contact Benedikt Schmid, MD, PhD
Phone +49 931 201 30309
Email schmid_b@ukw.de
Status Recruiting
Phase N/A
Start date March 28, 2022
Completion date February 28, 2024
View Details
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