Comparison of Conventional GlideScope to Single-Use GlideScope Cobalt for Orotracheal Intubation

NCT ID: NCT00459797

Last Updated: 2009-04-21

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

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-04-30

Study Completion Date

2008-08-31

Brief Summary

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Patients presenting for elective surgery requiring orotracheal intubation will be randomized to being intubated with either the conventional (reusable) GlideScope videolaryngoscope or the single-use GlideScope videolaryngoscope. The primary outcome is time to intubation.

Detailed Description

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Conditions

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Healthy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Conventional Glidescope

Group Type ACTIVE_COMPARATOR

Conventional (reusable) Glidescope

Intervention Type DEVICE

Single-use Glidescope

Group Type EXPERIMENTAL

Single-use Glidescope videolaryngoscope

Intervention Type DEVICE

Interventions

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Conventional (reusable) Glidescope

Intervention Type DEVICE

Single-use Glidescope videolaryngoscope

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Any patient who is ≥ 18 yrs. coming for elective surgery.
* Endotracheal tube is indicated for the procedure in the opinion of the attending anesthesiologist.
* Any operator who has performed ≥ 10 GlideScope intubations.

Exclusion Criteria

* Any patient in whom the use of the GlideScope is contraindicated in the opinion of the attending anesthesiologist.
* Any patient with cervical spine abnormalities.
* Any patients with known or probable difficult airways (this rare occurrence is unlikely to be evenly distributed between the groups and could skew the data).
* Any patient requiring rapid sequence induction.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

OTHER

Sponsor Role lead

Responsible Party

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LHSC

Principal Investigators

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Philip M Jones, MD

Role: PRINCIPAL_INVESTIGATOR

London Health Sciences Centre

Locations

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London Health Sciences Centre

London, Ontario, Canada

Site Status

Countries

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Canada

References

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Jones PM, Turkstra TP, Armstrong KP, Armstrong PM, Harle CC. Comparison of a single-use GlideScope Cobalt videolaryngoscope with a conventional GlideScope for orotracheal intubation. Can J Anaesth. 2010 Jan;57(1):18-23. doi: 10.1007/s12630-009-9204-9. Epub 2009 Oct 31.

Reference Type DERIVED
PMID: 19882199 (View on PubMed)

Other Identifiers

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13025

Identifier Type: -

Identifier Source: secondary_id

R-07-040

Identifier Type: -

Identifier Source: org_study_id

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