Comparison of McGrath and Macintosh Laryngoscopes for Insertion of a Double Lumen Tube by Residents

NCT ID: NCT03710096

Last Updated: 2022-11-04

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

148 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-11-04

Study Completion Date

2019-08-08

Brief Summary

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The insertion of double lumen tube is difficult even more if it is a resident with no experience. we think that using videolaryngoscopes for novice ones would facilitate insertion of double lumen tube thanks to the visualization on a LCD screen of the laryngeal structure.

Detailed Description

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Conditions

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Thoracic Injuries

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Mac grath group

Group Type EXPERIMENTAL

macGrath

Intervention Type DEVICE

in the mac grath group we use the videolaryngoscope macGrath as first-line for the insertion of double lumen tube

Macintosh Group

Group Type ACTIVE_COMPARATOR

Macintosh's

Intervention Type DEVICE

in the macintosh group we use the laryngoscope with Macintosh's blade as first-line for the insertion of double lumen tube

Interventions

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macGrath

in the mac grath group we use the videolaryngoscope macGrath as first-line for the insertion of double lumen tube

Intervention Type DEVICE

Macintosh's

in the macintosh group we use the laryngoscope with Macintosh's blade as first-line for the insertion of double lumen tube

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Thoracic Surgery
* Insertion of double lumen tube

Exclusion Criteria

* Emergency surgery
* Risk of inhalation
* Person unable to consent
* Persons deprived of liberty, under guardianship or trusteeship
* Pregnant or lactating woman
* Allergy to Tracrium, Propofol, Sufentanil
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Lille

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jacques Desbordes, MD,PhD

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Lille

Locations

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Hôpital Roger Salengro, CHU

Lille, , France

Site Status

Countries

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France

Other Identifiers

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2018-A00789-46

Identifier Type: OTHER

Identifier Source: secondary_id

2017_65

Identifier Type: -

Identifier Source: org_study_id

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