Skip to content

Evaluation of McGrath® MAC Video Laryngoscope

Evaluation of McGrath® MAC Using Glidescope® Ranger for Novice Providers in a Simulated Difficult Airway: A Randomised Manikin Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02051400
Acronym
EMMVL
Enrollment
39
Registered
2014-01-31
Start date
2013-09-30
Completion date
2013-11-30
Last updated
2014-01-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intubation; Difficult

Keywords

Intubation, Laryngoscopes

Brief summary

The purpose of this study is to evaluate whether the McGrath® MAC video laryngoscope is equal or superior when compared to the Glidescope® Ranger and the Macintosh laryngoscope for novice users in a simulated airway manikin.

Detailed description

Investigators compared two portable video laryngoscopes (the GlidesScope® Ranger (Verathon Inc, Bothell, WA, USA) and the McGrath® MAC (Aircraft Medical Ltd, Edinburgh, UK)) and a German type Macintosh metal blade with a fiberoptic light. A blade size of 4 was used on all devices. All intubations using video laryngoscopes were performed according to the manufacturers' instructions. A specialised rigid stylet (the GlideRite®) was used with the Glidescope® and a flexible plastic stylet bent with a hockey stick curvature, was used with the McGrath® MAC and the Macintosh laryngoscope. A size 7.5 endotracheal tube (Mallinckrodt™ Hi-Lo Oral/Nasal Tracheal Tube Cuffed Murphy Eye, Covidien, Ireland) was used with all the laryngoscopes. All participants were randomly divided into 3 device groups. Each group was allowed to attempt to perform endotracheal intubation five more times using the Laerdal® Airway Management Trainer (Laerdal Medical Korea Ltd., Seoul, Korea) with the normal airway setting. After completing the normal airway session, the participants performed another five attempts with the neck immobilisation setting using a neck collar. The sequence in which the three devices were used was randomly assigned, and all participants performed the same sequence at intervals of five weeks during the study.

Interventions

DEVICEthe McGrath® MAC video laryngoscope
DEVICEthe GlidesScope® Ranger video laryngoscope

Sponsors

Hanyang University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
22 Years to 33 Years
Healthy volunteers
Yes

Inclusion criteria

* Medical students without previous experience of intubation

Exclusion criteria

* Heart, wrist, or low back disease or who were pregnant were excluded

Design outcomes

Primary

MeasureTime frameDescription
Intubation parameter1st intubation attempt, an expected average of 1 min1. The rate for successful intubation 2. Time to intubation 3. The Cormack-Lehane grade at laryngoscopy

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026