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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03054272
Other study ID # Expertise-2016
Secondary ID
Status Completed
Phase N/A
First received February 7, 2017
Last updated May 1, 2017
Start date July 1, 2016
Est. completion date April 1, 2017

Study information

Verified date May 2017
Source Université de Montréal
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Using eye-tracking technology, the aim of this observational study is to compare the visual interests between attending physicians and residents watching a Cannot Intubate/Cannot Oxygenate (CICO) scripted and simulated scenario


Description:

Attending physicians and residents, from the department of Anesthesiology at the Université de Montréal were recruited on a voluntary basis. A 13-minute video based on a suggested CICO algorithm from the Difficult Airway Society to manage unanticipated difficult intubation in adults (3) was produced at the University of Montreal Simulation Centre using high-fidelity settings. The scenario was about a patient, with a cervical collar, in the post-anesthesia care unit. Throughout the video, the patient presents increasing respiratory distress worsening to respiratory failure. The anesthesiologist fails to ventilate, intubate and insert a laryngeal mask leading to a cricothyroidotomy. All participants were looking at a screen on which the scenario was broadcast. The screen was equipped with TobiiEyeX®, an eye-tracking system that automatically aggregates gaze data.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date April 1, 2017
Est. primary completion date February 1, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Residents and attending physicians from University of Montreal Anesthesia Department

Exclusion Criteria:

Study Design


Intervention

Behavioral:
Video
A 13-minute video based on a suggested CICO algorithm from the Difficult Airway Society that was produced at the University of Montreal Simulation Centre using high-fidelity settings.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Université de Montréal

Outcome

Type Measure Description Time frame Safety issue
Primary Difference between Time to First Fixation and Total View Duration of areas of interests. The screen was equipped with TobiiEyeX®, an eye-tracking system that automatically aggregates gaze data. The display was divided in seven Areas of Interest (AOI). Data were collected using the Tobii Studio® program to obtain the total view duration (TVD) of the various AOIs. The primary endpoint is collected during 15 minutes, throughout the viewing of the video by the participant
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