Facilitated By

San Antonio Medical Foundation

Direct Versus Video Laryngoscope (DEVICE) Airway Trial

59th Medical Wing at the Wilford Hall Ambulatory Surgical Center (WHASC)

The 59th Medical Wing at the Wilford Hall Ambulatory Surgical Center (WHASC) provides support for research conducted by investigators and their collaborators addressing the unique scientific needs of the Air Force, the Department of Defense and the Nation.

Principal Investigator(s)
Maj Steven Schauer
Col Vic Bebarta
Funded by
J9 Restoral
Research Start Date
Status
Active

We propose a multicenter, non-blinded, parallel-group, randomized clinical trial (RCT) evaluating the effect of video versus direct laryngoscope use on successful first attempt tracheal intubations. Adult patients in participating EDs and ICUs who require tracheal intubation and who meet eligibility criteria will be enrolled and randomly assigned to either a video or direct laryngoscope for the first intubation attempt. The video laryngoscope group operators will use the video screen on the first attempt. All other decisions regarding airway management will remain at the discretion of the treating physician. An independent observer will prospectively collect all data at the time of intubation. We will supplement this prospective data collection with review of the medical record to determine the effect of the assigned interventions on study outcomesWe propose a multicenter, non-blinded, parallel-group, randomized clinical trial (RCT) evaluating the effect of video versus direct laryngoscope use on successful first attempt tracheal intubations. Adult patients in participating EDs and ICUs who require tracheal intubation and who meet eligibility criteria will be enrolled and randomly assigned to either a video or direct laryngoscope for the first intubation attempt. The video laryngoscope group operators will use the video screen on the first attempt. All other decisions regarding airway management will remain at the discretion of the treating physician. An independent observer will prospectively collect all data at the time of intubation. We will supplement this prospective data collection with review of the medical record to determine the effect of the assigned interventions on study outcomes.

Collaborative Project
Medical Devices
Other
The views expressed are those of the authors and do not reflect the official views or policy of the Department of Defense or its Components. Where applicable, the voluntary fully informed consent of the subjects used in this research was obtained as required by 32 CFR 219 and DODI 3216.02_AFI 40-402