GlideScope Groove vs. Standard GlideScope: A Non-inferiority Study
NCT ID: NCT01489605
Last Updated: 2019-02-28
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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WITHDRAWN
NA
INTERVENTIONAL
2019-07-31
2020-06-30
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
TRIPLE
Study Groups
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GlideScope Groove
Patients will be intubated using the GlideScope Groove device. (Verathon)
GlideScope Groove
Patients will be intubated using the GlideScope Groove device. (Verathon)
Control: Standard GlideScope
Control: Patients will be intubated using standard practice, a standard GlideScope (Verathon)
Control: Standard GlideScope
Patients will be intubated using the standard GlideScope. (Verathon)
Interventions
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GlideScope Groove
Patients will be intubated using the GlideScope Groove device. (Verathon)
Control: Standard GlideScope
Patients will be intubated using the standard GlideScope. (Verathon)
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
2. Any patients with known or probable difficult airways.
3. Any patient requiring rapid sequence induction.
18 Years
85 Years
ALL
Yes
Sponsors
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University of Western Ontario, Canada
OTHER
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
OTHER
Responsible Party
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Timothy Turkstra
Staff Anesthesiologist and Associate Professor
Principal Investigators
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Timothy Turkstra, MD, M. Eng
Role: PRINCIPAL_INVESTIGATOR
UWO
Locations
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London Health Sciences Center University Hospital
London, Ontario, Canada
London Health Sciences Centre Victoria Campus
London, Ontario, Canada
Countries
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Other Identifiers
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18477
Identifier Type: -
Identifier Source: org_study_id
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