Comparison of AirTraq Laryngoscope to Macintosh Laryngoscope for Intubation of Patients With Potential Cervical Spine Injury
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Purpose
Intubation is frequently required for trauma patients as part of the resuscitative effort. When the stability of the cervical spine is unknown, the potential for spinal cord damage during intubation is significant; the question of the safest intubating technique has not been resolved. Previous Studies have evaluated Macintosh Laryngoscopy, Bullard Laryngoscope, face mask ventilation, fibre-optic guided oral and nasal intubation, esophageal Combitube®, Laryngeal Mask Airway® (LMA), and Intubating Laryngeal Mask Airway® (ILMA) use with respect to cervical spine movement. Our previous study evaluated the Intubating Lighted Stylet (Lightwand®) and GlideScope® versus the Macintosh Laryngoscope.
Another method of securing endotracheal intubation, approved and in routine use, is the AirTraq® videolaryngoscope (ProMedic, Inc, Bonita Springs, FL, USA). The AirTraq videolaryngoscope is a videolaryngoscope with an external video display of the glottic opening and an endotracheal tube track to guide the ETT through the vocal cords (www.airtraq.com). When a clear view of the vocal cords is obtained, the endotracheal tube may be advanced into the trachea. This technique can be performed rapidly and safely and there is the perception that it involves less cervical spine movement than direct laryngoscopy.
We propose to study the AirTraq videolaryngoscope to determine if its use would result in reduced cervical spine movement during intubation.
| Condition | Intervention |
|---|---|
|
Trauma |
Device: AirTraq |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Crossover Assignment Masking: Open Label Primary Purpose: Health Services Research |
| Official Title: | Comparison of AirTraq Laryngoscope to Macintosh Laryngoscope for Intubation of Patients With Potential Cervical Spine Injury |
- Cervical Spine Movement [ Time Frame: Intubation ] [ Designated as safety issue: No ]
- Time to Intubation [ Time Frame: Intubation ] [ Designated as safety issue: No ]
| Enrollment: | 24 |
| Study Start Date: | January 2008 |
| Study Completion Date: | May 2008 |
| Primary Completion Date: | May 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
Air Traq then Macintosh
|
Device: AirTraq
Laryngoscopy with AirTraq
|
|
Experimental: 2
Macintosh then AirTraq
|
Device: AirTraq
Laryngoscopy with AirTraq
|
Show Detailed Description
Eligibility| Ages Eligible for Study: | 18 Years to 75 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Elective non-cardiac surgery patients requiring intubation for the surgery.
- (Cardiac surgery uses TEE; there would not be space for the fluoroscopy machine.)
- ASA 1-3
- Body Mass Index (BMI) < 35
Exclusion Criteria:
- patients with previous neck surgery or unstable C-spine
- patients with Reflux disease (GERD)
- patients who are or may be pregnant
Contacts and Locations| Canada, Ontario | |
| University of Western Ontario | |
| London, Ontario, Canada, N6A 5A5 | |
| Principal Investigator: | Timothy P Turkstra, MD | University of Western Ontario, Canada |
More Information
No publications provided
| Responsible Party: | T. P. Turkstra, University of Western Ontario |
| ClinicalTrials.gov Identifier: | NCT00664612 History of Changes |
| Other Study ID Numbers: | R-07-337, 13481 |
| Study First Received: | April 18, 2008 |
| Last Updated: | October 15, 2008 |
| Health Authority: | Canada: Ethics Review Committee |
Keywords provided by Lawson Health Research Institute:
|
Cervical Spine |
Additional relevant MeSH terms:
|
Spinal Injuries Back Injuries Wounds and Injuries |
ClinicalTrials.gov processed this record on May 16, 2013