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GlideScope Groove vs. Standard GlideScope: A Non-inferiority Study

NCT01489605 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2019-02-28

No results posted yet for this study

Summary

Patients presenting for elective surgery requiring orotracheal intubation will be randomized to being intubated with either the GlideScope Groove video-laryngoscope or the standard GlideScope video-laryngoscope.

Conditions

  • Intubation, Orotracheal

Interventions

DEVICE

GlideScope Groove

Patients will be intubated using the GlideScope Groove device. (Verathon)

DEVICE

Control: Standard GlideScope

Patients will be intubated using the standard GlideScope. (Verathon)

Sponsors & Collaborators

  • University of Western Ontario, Canada

    collaborator OTHER

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

    lead OTHER

Principal Investigators

  • Timothy Turkstra, MD, M. Eng · UWO

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-07-31
Primary Completion
2020-06-30
Completion
2020-06-30

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01489605 on ClinicalTrials.gov