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| Sponsor: | Lawson Health Research Institute |
|---|---|
| Collaborator: |
London Health Sciences Centre |
| Information provided by: | Lawson Health Research Institute |
| ClinicalTrials.gov Identifier: | NCT00400972 |
Purpose
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.
| Condition | Intervention |
|---|---|
|
Nasal Intubation |
Device: GlideScope videolaryngoscope |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Single Blind, Active Control, Single Group Assignment, Safety/Efficacy Study |
| Official Title: | Comparison of GlideScope Videolaryngoscopy to Direct Laryngoscopy for Nasal Intubation |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Canada, Ontario | |
| London Health Sciences Centre | |
| London, Ontario, Canada, N6A5A5 | |
| Principal Investigator: | Philip M Jones, MD | London Health Sciences Centre |
More Information
| Study ID Numbers: | R-06-467, HSREB 12719 |
| Study First Received: | November 15, 2006 |
| Last Updated: | September 27, 2007 |
| ClinicalTrials.gov Identifier: | NCT00400972 History of Changes |
| Health Authority: | Canada: Ethics Review Committee |
|
GlideScope videolaryngoscopy intubation nasal |
nasotracheal laryngoscopy anesthesia |