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

NCT ID: NCT04087135

Last Updated: 2019-09-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

25 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-03-11

Study Completion Date

2019-06-30

Brief Summary

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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

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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.

Conditions

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Laryngoscope Hemoptysis Simulation Cadaver Intubation; Difficult or Failed

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Each participant will performe the intubation three time using the tools provided, for the same simulation situation: (a) direct laryngoscopy, (b) videolaryngoscopy McGrath and (c) videolaryngoscopy McGrath with suction.
Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants

Study Groups

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participant LD

Group Type EXPERIMENTAL

direct laryngoscopy

Intervention Type OTHER

Participants will intubate the hemoptysis cadaver model in simulation with direct laryngoscopy MacIntosh blade.

participant VL

Group Type EXPERIMENTAL

videolaryngoscopy McGrath

Intervention Type OTHER

Participants will intubate the hemoptysis cadaver model in simulation with videolaryngoscopy using McGrath and the short curved blade (XBlade)

participant VLS

Group Type EXPERIMENTAL

videolaryngoscopy McGrath with suction

Intervention Type OTHER

Participants will intubate the hemoptysis cadaver model in simulation with videolaryngoscopy using McGrath and the short curved blade (XBlade) and a suction they will advanced directly before the optic of the camera.

Interventions

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direct laryngoscopy

Participants will intubate the hemoptysis cadaver model in simulation with direct laryngoscopy MacIntosh blade.

Intervention Type OTHER

videolaryngoscopy McGrath

Participants will intubate the hemoptysis cadaver model in simulation with videolaryngoscopy using McGrath and the short curved blade (XBlade)

Intervention Type OTHER

videolaryngoscopy McGrath with suction

Participants will intubate the hemoptysis cadaver model in simulation with videolaryngoscopy using McGrath and the short curved blade (XBlade) and a suction they will advanced directly before the optic of the camera.

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Centre d'Apprentissage des Habiletés Cliniques (CAAHC)

UNKNOWN

Sponsor Role collaborator

Laboratoire d'anatomie de Trois-Rivières

UNKNOWN

Sponsor Role collaborator

Université de Montréal

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Hôpital Trois-Rivières

Trois-Rivières, Quebec, Canada

Site Status

Countries

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Canada

Other Identifiers

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HP2018

Identifier Type: -

Identifier Source: org_study_id

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