Comparison Study in Adult Surgical Patients of 5 Airway Devices
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| ClinicalTrials.gov Identifier: NCT00602979 |
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Recruitment Status :
Completed
First Posted : January 28, 2008
Results First Posted : May 19, 2017
Last Update Posted : May 19, 2017
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Laryngoscopy Intubation | Device: Macintosh laryngoscope Device: Airtraq® Optical Laryngoscope Device: Storz DCI Video Laryngoscope® Device: GlideScope® Video Laryngoscope Device: McGRATH® Video Laryngoscope | Not Applicable |
Historically, optical and video laryngoscopes have been used as alternative airway management devices for the difficult airway, and as rescue devices. Their use by experienced laryngoscopists has not been compared in a prospective, randomized, head-to-head comparison for routine airway management in adult surgical patients. Video and optical laryngoscopes have been developed to improve the laryngeal view for tracheal intubation and to decrease physiological stress associated with the procedure. The objective of this study is to determine whether these devices offer superior intubating conditions for routine surgical management, over the Macintosh laryngoscope, which is the current standard. The devices to be compared in this study are the most commonly used video and optical laryngoscopes on the market and are cleared or exempt by the Food and Drug Administration (FDA).
Eligible subjects include elective adult surgical patients with an ASA status between 1 and 3 requiring general endotracheal anesthesia. Subjects with a BMI ≥ 40, or undergoing surgery in close proximity to the neck will be excluded. Prior to surgery, subjects will receive a pre-anesthesia evaluation with particular attention to the airway using the Mallampati classification system; atlanto-occipital joint extension; thyro-mental distance; temporomandibular joint function; inter-incisor distance; and dental assessment. Subjects will be randomized for intubation with one of the five laryngoscopes in equal proportions. The following data were recorded: total intubation time, maximum neck extension using an angle gauge, glottic view, assessed by the anesthesiologist using the Cook modification of the Cormack-Lehane grading system (Figure 1), and ease of tracheal intubation using a 5-point rating scale; 5 (excellent) to 1 (poor). Subjects were queried about soreness or painful swallowing in the PACU and a week later via a phone call.
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 240 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Single (Participant) |
| Primary Purpose: | Supportive Care |
| Official Title: | Prospective, Randomized Comparison of Intubating Conditions With Airtraq Optical, Storz DCI Video, McGRATH Video, GlideScope Video, & Macintosh Laryngoscope in Randomly Selected Elective Adult Surgical Patients |
| Study Start Date : | April 2008 |
| Actual Primary Completion Date : | September 2009 |
| Actual Study Completion Date : | July 2011 |
| Arm | Intervention/treatment |
|---|---|
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Macintosh laryngoscope
Macintosh laryngoscope (control group/direct laryngoscopy) - current standard
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Device: Macintosh laryngoscope
Used during laryngoscopy to facilitate intubation. |
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Airtraq Optical Laryngoscope
Airtraq® Optical Laryngoscope (an experimental group/indirect laryngoscopy)
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Device: Airtraq® Optical Laryngoscope
Used during laryngoscopy to facilitate intubation. |
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Storz DCI Video Laryngoscope
Storz DCI Video Laryngoscope® (an experimental group/indirect laryngoscopy)
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Device: Storz DCI Video Laryngoscope®
Used during laryngoscopy to facilitate intubation |
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GlideScope Video Laryngoscope
GlideScope® Video Laryngoscope (an experimental group/indirect laryngoscopy)
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Device: GlideScope® Video Laryngoscope
Used during laryngoscopy to facilitate intubation |
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McGRATH Video Laryngoscope
McGRATH® Video Laryngoscope (an experimental group/indirect laryngoscopy)
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Device: McGRATH® Video Laryngoscope
Used during laryngoscopy to facilitate intubation |
- Percentage Distribution of Cook's Modification of Cormack-Lehane's Grading System. Each Study Subject Will Receive a Grade of 1, 2A, 2B, 3A, 3B, or 4 in the Cormack-Lehane Grading System. [ Time Frame: 1 time during laryngoscopy ]
Percentage distribution of Cook's modification of Cormack-Lehane's grading system. This is a classification that records the best laryngeal view obtained with or without anterior laryngeal pressure. Each study subject will receive a grade of 1, 2A, 2B, 3A, 3B, or 4 in the Cormack-Lehane grading system. Grades 1 and 2A classify as an easy view: when the laryngeal inlet is visible. Grades 2B and 3A classify as restricted: when the posterior glottic structures are visible or the epiglottis is visible and can be lifted. Grades 3B and 4 classify as difficult: when the epiglottis cannot be lifted or when no laryngeal structures are visible.
Cook's modification of Cormack-Lehane's Grades 1=1, 2=2A,3=2B, 4=3A, 5=3B, 6=4.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Elective adult surgical patient requiring general endotracheal anesthesia.
- Males and Females.
- ASA Physical Status 1-3.
- Age 18 years of age and older
Exclusion Criteria:
- Body Mass Index (BMI) ≥35kg/m2.
- If subject is of childbearing potential, a positive pregnancy test at the time of study enrollment.
- Has physical, mental, or medical conditions which, in the opinion of the Investigator, could compromise the subject's welfare, ability to communicate with the study staff, complete study activities, or would otherwise contraindicate study participation.
- Intubated prior to surgery.
- Severe cardiovascular, hepatic or renal disease.
- Need for nasal intubation.
- An investigator of this study.
- Inclusion in another clinical research study.
- Subject's refusal or inability to agree to and to sign the Informed Consent Form in English.
- Subject requiring awake airway management.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00602979
| Principal Investigator: | Jon Samuels, MD | Weill Medical College of Cornell University |
| Responsible Party: | Weill Medical College of Cornell University |
| ClinicalTrials.gov Identifier: | NCT00602979 |
| Other Study ID Numbers: |
0710009433 |
| First Posted: | January 28, 2008 Key Record Dates |
| Results First Posted: | May 19, 2017 |
| Last Update Posted: | May 19, 2017 |
| Last Verified: | April 2017 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
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endotracheal intubation intubation laryngoscopy laryngoscope surgery |

