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

Sponsor
Université de Montréal (Other)
Overall Status
Completed
CT.gov ID
NCT04087135
Collaborator
Centre d'Apprentissage des Habiletés Cliniques (CAAHC) (Other), Laboratoire d'anatomie de Trois-Rivières (Other)
25
1
3
3.6
6.9

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: direct laryngoscopy
  • Other: videolaryngoscopy McGrath
  • Other: videolaryngoscopy McGrath with suction
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
25 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Intervention Model Description:
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.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.
Masking:
Single (Participant)
Primary Purpose:
Other
Official Title:
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
Actual Study Start Date :
Mar 11, 2019
Actual Primary Completion Date :
Jun 30, 2019
Actual Study Completion Date :
Jun 30, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: participant LD

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

Experimental: participant VL

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

Experimental: participant VLS

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.

Outcome Measures

Primary Outcome Measures

  1. failure of intubation on first try [the duration of the simulation]

    defined as the withdrawal of the laryngoscope from the mouth

Secondary Outcome Measures

  1. time to intubation [the duration of the simulation]

    from the insertion of the laryngoscope in the mouth to the inflation of the endotracheal cuff

  2. failure in intubation [the duration of the simulation]

    failure to intubate after three try

  3. use of suction [the duration of the simulation]

    document the use of suction

  4. difficulty of intubation [the duration of the simulation]

    as describe by the participants on a Likert scale 1 to 5

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hôpital Trois-Rivières Trois-Rivières Quebec Canada H2J3T5

Sponsors and Collaborators

  • Université de Montréal
  • Centre d'Apprentissage des Habiletés Cliniques (CAAHC)
  • Laboratoire d'anatomie de Trois-Rivières

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Université de Montréal
ClinicalTrials.gov Identifier:
NCT04087135
Other Study ID Numbers:
  • HP2018
First Posted:
Sep 12, 2019
Last Update Posted:
Sep 12, 2019
Last Verified:
Oct 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Université de Montréal
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 12, 2019