Comparison of Conventional GlideScope to Single-Use GlideScope Cobalt for Orotracheal Intubation
NCT ID: NCT00459797
Last Updated: 2009-04-21
Study Results
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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COMPLETED
NA
100 participants
INTERVENTIONAL
2007-04-30
2008-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Conventional Glidescope
Conventional (reusable) Glidescope
Single-use Glidescope
Single-use Glidescope videolaryngoscope
Interventions
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Conventional (reusable) Glidescope
Single-use Glidescope videolaryngoscope
Eligibility Criteria
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Inclusion Criteria
* 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 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.
18 Years
ALL
Yes
Sponsors
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London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
OTHER
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
Countries
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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.
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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