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Clinical Trials/NCT02787629
NCT02787629
Completed
Not Applicable

Comparison of Simultaneous Endotracheal Tube Insertion With GlideScope Use: a Pilot Study

Lawson Health Research Institute2 sites in 1 country50 target enrollmentOctober 1, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Intubation
Sponsor
Lawson Health Research Institute
Enrollment
50
Locations
2
Primary Endpoint
Duration of Intubation
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Patients presenting for elective surgery requiring orotracheal intubation will be randomized to having the ETT inserted into the pharynx simultaneous to GlideScope insertion and then having the ETT advanced under GlideScope guidance into the trachea, or, being intubated in the more common fashion with the GlideScope being inserted first and having the ETT then advanced via the pharynx into the trachea.

Detailed Description

Patients presenting for elective surgery requiring orotracheal intubation will be randomized to having the ETT inserted into the pharynx simultaneous to GlideScope insertion and then having the ETT advanced under GlideScope guidance into the trachea, or, being intubated in the more common fashion with the GlideScope being inserted first and having the ETT then advanced via the pharynx into the trachea. The primary outcome is time to intubation. Secondary outcomes include: 1) Ease of intubation as noted by operator (measured on a 10-cm Visual Analogue Scale) 2) Number of intubation attempts 3) Number of failures to intubate 4) Use of external laryngeal pressure 5) Laryngoscopic grade distribution

Registry
clinicaltrials.gov
Start Date
October 1, 2016
End Date
June 30, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adult patient booked for elective surgery requiring orotracheal intubation

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.
  • Any patient requiring rapid sequence induction.

Outcomes

Primary Outcomes

Duration of Intubation

Time Frame: During the intubation

Duration of Intubation from mask removal to confirmation of ETCO2

Secondary Outcomes

  • Ease of Intubation(Within 5 minutes of the completion of the intubation)
  • Number of intubation attempts(Within 5 minutes of the completion of the intubation)
  • Failure to intubate(Within 5 minutes of the completion of the intubation)
  • Oropharyngeal Trauma(Within 5 minutes of the completion of the intubation)
  • Laryngoscopic Grade(Within 5 minutes of the completion of the intubation)

Study Sites (2)

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