Trials / Withdrawn
WithdrawnNCT01489605
GlideScope Groove vs. Standard GlideScope: A Non-inferiority Study
Comparison of GlideScope Groove to Standard GlideScope for Orotracheal Intubation: A Non-inferiority Study
- Status
- Withdrawn
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's · Academic / Other
- Sex
- All
- Age
- 18 Years – 85 Years
- Healthy volunteers
- Accepted
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.
Detailed description
See above. The primary outcome is time to intubation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | GlideScope Groove | Patients will be intubated using the GlideScope Groove device. (Verathon) |
| DEVICE | Control: Standard GlideScope | Patients will be intubated using the standard GlideScope. (Verathon) |
Timeline
- Start date
- 2019-07-01
- Primary completion
- 2020-06-01
- Completion
- 2020-06-01
- First posted
- 2011-12-09
- Last updated
- 2019-02-28
Locations
2 sites across 1 country: Canada
Source: ClinicalTrials.gov record NCT01489605. Inclusion in this directory is not an endorsement.