Comparison of GlideScope Videolaryngoscopy to Direct Laryngoscopy for Nasal Intubation - Tabular View

Tracking Information

First Received Date ^ICMJE

November 15, 2006

Last Updated Date

September 27, 2007

Start Date ^ICMJE

November 2006

Primary Completion Date

Current Primary Outcome Measures ^ICMJE

time to intubation

Original Primary Outcome Measures ^ICMJE

Same as current

Change History

Complete list of historical versions of study NCT00400972 on ClinicalTrials.gov Archive Site

Current Secondary Outcome Measures ^ICMJE

ease of intubation (VAS)
incidence of trauma
number of failures
severity of patient sore throat on post-operative day 1

Original Secondary Outcome Measures ^ICMJE

Same as current

Descriptive Information

Brief Title ^ICMJE

Comparison of GlideScope Videolaryngoscopy to Direct Laryngoscopy for Nasal Intubation

Official Title ^ICMJE

Comparison of GlideScope Videolaryngoscopy to Direct Laryngoscopy for Nasal Intubation

Brief Summary

The purpose of this study is to determine whether nasal intubation assisted by GlideScope videolaryngoscopy is faster, easier, and less traumatic than nasal intubation with conventional direct laryngoscopy.

Detailed Description

Study Phase

Study Type ^ICMJE

Interventional

Study Design ^ICMJE

Treatment, Randomized, Single Blind, Active Control, Single Group Assignment, Safety/Efficacy Study

Condition ^ICMJE

Nasal Intubation

Intervention ^ICMJE

Device: GlideScope videolaryngoscope

Study Arms / Comparison Groups

Publications *

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information

Recruitment Status ^ICMJE

Completed

Estimated Enrollment ^ICMJE

Completion Date

September 2007

Primary Completion Date

Eligibility Criteria ^ICMJE

Inclusion Criteria:

any patient who is at least 18 years old
patient requires nasal intubation for surgical indications
operator has performed at least 10 prior GlideScope intubations (oral or nasal)

Exclusion Criteria:

cervical spine abnormalities
known difficult airway
requires rapid sequence induction
any other patient in whom the attending anesthesiologist believes usage of the GlideScope is contraindicated

Gender

Both

Ages

18 Years and older

Accepts Healthy Volunteers

Yes

Contacts ^ICMJE

Contact information is only displayed when the study is recruiting subjects

Location Countries ^ICMJE

Canada

Administrative Information

NCT ID ^ICMJE

NCT00400972

Responsible Party

Study ID Numbers ^ICMJE

R-06-467, HSREB 12719

Study Sponsor ^ICMJE

Lawson Health Research Institute

Collaborators ^ICMJE

London Health Sciences Centre

Investigators ^ICMJE

Principal Investigator:

Philip M Jones, MD

London Health Sciences Centre

Information Provided By

Lawson Health Research Institute

Verification Date

September 2007

^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP