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Comparison of Early Endotracheal Tube Insertion With GlideScope Use

Comparison of Early Endotracheal Tube Insertion With GlideScope Use

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01564082
Enrollment
160
Registered
2012-03-27
Start date
2012-04-30
Completion date
2013-03-31
Last updated
2015-04-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endotracheal Intubation

Keywords

endotracheal intubation, GlideScope

Brief summary

Patients presenting for elective surgery will be randomized to having the breathing tube inserted partly into the throat prior to GlideScope insertion, or having it inserted fully after GlideScope insertion.

Detailed description

Patients presenting for elective surgery requiring orotracheal intubation will be randomized to having the Early Endotracheal Tube (ETT) inserted into the pharynx prior to GlideScope insertion and then having the ETT advanced under GlideScope guidance into the trachea, or, being intubated in the standard 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.

Interventions

DEVICEETT First (GlideScope)

Patients will have the endotracheal tube (ETT) introduced into the pharynx under direct vision prior to GlideScope insertion. The ETT will then be advanced under GlideScope guidance into the trachea.

Sponsors

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

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

1. Any adult patient booked for elective surgery requiring orotracheal intubation. 2. Any operator who has performed ≥ 20 GlideScope intubations.

Exclusion criteria

1. Any patient in whom the use of the GlideScope is contraindicated in the opinion of the attending anesthesiologist. 2. Any patient with cervical spine abnormalities. 3. Any patients with known or probable difficult airways. 4. Any patient requiring rapid sequence induction.

Design outcomes

Primary

MeasureTime frameDescription
Time to IntubationDay 1Duration of intubation of the patient

Secondary

MeasureTime frameDescription
Ease of intubationDay 1Ease of intubation, measured on a Visual analog scale
Number of intubation attemptsDay 1Number of intubation attempts
Use of external laryngeal pressureDay 1Use of external laryngeal pressure
Sore throatDay 3Post operative sore throat, as rated by the patient.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026