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Clinical Trials/NCT04087135
NCT04087135
Completed
Not Applicable

Comparison of the Success Rate of Intubation With Direct Laryngoscopy or Videolaryngoscopy in an Hemoptysis Simulated Situation on Human Cadaver Embalmed With Thiel's Method

Université de Montréal1 site in 1 country25 target enrollmentMarch 11, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Laryngoscope
Sponsor
Université de Montréal
Enrollment
25
Locations
1
Primary Endpoint
failure of intubation on first try
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Our study first aims to develope a realistic cadaver model of hemoptysis based on Thiel's embalmed cadavers. Secondly, participants will intubate the hemoptysis cadaver model with (a) the direct laryngoscopy with MacIntosh blade, (b) the videolaryngoscopy with McGrath XBlade and (c) the videolaryngoscopy with McGrath XBlade and a suction advance before the optic of the camera. We hypothesis that, in simulated hemoptysis on the Thiel's embalmed cadaver, the rate of failed intubation at first try will be different depending on the laryngoscope used.

Detailed Description

For the simulation of hemoptysis, we will need to use the Thiel's embalmed cadaver, who's realism is established, create a synthetic form of blood resembling real blood by its viscosity and color for the simulation and elaborate the dynamic interface of the simulation of hemoptysis. The quantity and way of administration of the blood through the trachea will be tested to obtain a realistic hemoptysis as seen in supraglottic. For the simulation, we will compare the efficiency of intubation, judged by the failure rate of intubation on first try, for (a) the direct laryngoscopy with MacIntosh blade, (b) the videolaryngoscopy with McGrath XBlade and (c) the videolaryngoscopy with McGrath XBlade with the suction advanced before the camera. We will also measure the time to intubation, the failure rate of intubation, the suction use and the difficulty of intubation as reported by the participants.

Registry
clinicaltrials.gov
Start Date
March 11, 2019
End Date
June 30, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • all wiling doctors and medical residents in the departments of anesthesiology, emergency medicine and intensive care
  • experience with the technique of intubation using videolaryngoscopy and direct laryngoscopy.

Exclusion Criteria

  • refusal to participate

Outcomes

Primary Outcomes

failure of intubation on first try

Time Frame: the duration of the simulation

defined as the withdrawal of the laryngoscope from the mouth

Secondary Outcomes

  • time to intubation(the duration of the simulation)
  • failure in intubation(the duration of the simulation)
  • use of suction(the duration of the simulation)
  • difficulty of intubation(the duration of the simulation)

Study Sites (1)

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