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

Not Applicable
Withdrawn
Conditions
Intubation, Orotracheal
Interventions
Device: GlideScope Groove
Registration Number
NCT01489605
Lead Sponsor
Lawson Health Research Institute
Brief 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.

Detailed Description

See above. The primary outcome is time to intubation.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Any adult patient booked for elective surgery requiring orotracheal intubation.
Exclusion Criteria
  1. Any patient with cervical spine abnormalities.
  2. Any patients with known or probable difficult airways.
  3. Any patient requiring rapid sequence induction.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
GlideScope GrooveGlideScope GroovePatients will be intubated using the GlideScope Groove device. (Verathon)
Primary Outcome Measures
NameTimeMethod
Duration of IntubationDay 1

Duration of Intubation - Mask removal to ETCO2 confirmation

Secondary Outcome Measures
NameTimeMethod
Sore ThroatDay 3

Patients will be surveyed with respect to the incidence of post-operative sore throat.

Incidence of traumaDay 1

Incidence of trauma

Ease of intubationDay 1

Ease of intubation as noted by operator (measured on a 100 mm Visual Analogue Scale)

Number of failures to intubateDay 1

Number of failures to intubate

Use of external laryngeal pressureDay 1

Use of external laryngeal pressure

Laryngoscopic grade distributionDay 1

Laryngoscopic grade distribution according to Cormack and Lehane classification

Trial Locations

Locations (2)

London Health Sciences Center University Hospital

🇨🇦

London, Ontario, Canada

London Health Sciences Centre Victoria Campus

🇨🇦

London, Ontario, Canada

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