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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02787629
Other study ID # 107322
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2016
Est. completion date June 30, 2018

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 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.


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


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date June 30, 2018
Est. primary completion date June 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

1) Adult patient booked for elective surgery requiring orotracheal intubation

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.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Simultaneous Intubation
Intubation with GlideScope and ETT inserted simultaneously
Standard Intubation
Intubation with GlideScope inserted first and ETT insertion after the GlideScope view is obtained

Locations

Country Name City State
Canada London Health Sciences Center University Hospital London Ontario
Canada St. Joseph's Health Care London Ontario

Sponsors (1)

Lead Sponsor Collaborator
Lawson Health Research Institute

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Duration of Intubation Duration of Intubation from mask removal to confirmation of ETCO2 During the intubation
Secondary Ease of Intubation 100 mm visual analog scale Within 5 minutes of the completion of the intubation
Secondary Number of intubation attempts Number of intubation attempts Within 5 minutes of the completion of the intubation
Secondary Failure to intubate Failure to intubate Within 5 minutes of the completion of the intubation
Secondary Laryngoscopic Grade Cormack & Lehane grade Within 5 minutes of the completion of the intubation
Secondary Oropharyngeal Trauma Blind suction of the oropharynx immediately post intubation Within 5 minutes of the completion of the intubation
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