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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01489605
Other study ID # 18477
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date July 2019
Est. completion date June 2020

Study information

Verified date February 2019
Source Lawson Health Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Description:

See above. The primary outcome is time to intubation.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 2020
Est. primary completion date June 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 85 Years
Eligibility 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


Related Conditions & MeSH terms


Intervention

Device:
GlideScope Groove
Patients will be intubated using the GlideScope Groove device. (Verathon)
Control: Standard GlideScope
Patients will be intubated using the standard GlideScope. (Verathon)

Locations

Country Name City State
Canada London Health Sciences Center University Hospital London Ontario
Canada London Health Sciences Centre Victoria Campus London Ontario

Sponsors (2)

Lead Sponsor Collaborator
Lawson Health Research Institute University of Western Ontario, Canada

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Duration of Intubation Duration of Intubation - Mask removal to ETCO2 confirmation Day 1
Secondary Ease of intubation Ease of intubation as noted by operator (measured on a 100 mm Visual Analogue Scale) Day 1
Secondary Incidence of trauma Incidence of trauma Day 1
Secondary Number of failures to intubate Number of failures to intubate Day 1
Secondary Use of external laryngeal pressure Use of external laryngeal pressure Day 1
Secondary Laryngoscopic grade distribution Laryngoscopic grade distribution according to Cormack and Lehane classification Day 1
Secondary Sore Throat Patients will be surveyed with respect to the incidence of post-operative sore throat. Day 3