NCT00400972

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Nov 2006

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2006

Completed
14 days until next milestone

First Submitted

Initial submission to the registry

November 15, 2006

Completed
2 days until next milestone

First Posted

Study publicly available on registry

November 17, 2006

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2007

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2007

Completed
Last Updated

October 29, 2021

Status Verified

September 1, 2007

Enrollment Period

10 months

First QC Date

November 15, 2006

Last Update Submit

October 28, 2021

Conditions

Nasal Intubation

Keywords

GlideScopevideolaryngoscopyintubationnasalnasotracheallaryngoscopyanesthesia

Outcome Measures

Primary Outcomes (1)

  • time to intubation

Secondary Outcomes (4)

  • ease of intubation (VAS)

  • incidence of trauma

  • number of failures

  • severity of patient sore throat on post-operative day 1

Interventions

GlideScope videolaryngoscopeDEVICE

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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)

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

London Health Sciences Centre

London, Ontario, N6A5A5, Canada

Location

Study Officials

  • Philip M Jones, MD

    London Health Sciences Centre

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER

Study Record Dates

First Submitted

November 15, 2006

First Posted

November 17, 2006

Study Start

November 1, 2006

Primary Completion

September 1, 2007

Study Completion

September 1, 2007

Last Updated

October 29, 2021

Record last verified: 2007-09

Locations

CA(1)