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CompletedNCT02051400EMMVLUpdated Jan 31, 2014

Evaluation of McGrath® MAC Video Laryngoscope

An interventional study of the McGrath® MAC video laryngoscope and the GlidesScope® Ranger video laryngoscope in Intubation; Difficult, sponsored by Hanyang University. Completed at 1 site in Korea, Republic of. Open to participants aged 22 Years to 33 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2014-01-31.

Sponsored by Hanyang University · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
39
Allocation
Randomized
Ages
22 Years to 33 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Intubation; Difficult

Keywords

  • Intubation
  • Laryngoscopes
03

In context

Lead sponsor

Hanyang University is the lead sponsor of 51 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
22 Years to 33 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Medical students without previous experience of intubation

Exclusion criteria

Exclusion Criteria:

  • Heart, wrist, or low back disease or who were pregnant were excluded
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
39 participants (actual)

Study arms

  • Experimental
    Intubation with the McGrath® MAC video laryngoscope

    Participants perform five intubation attempts using the airway manikin with the normal airway setting. After completing the normal airway session, the participants performed another five attempts with the neck immobilization setting using a neck collar.

    Device: the McGrath® MAC video laryngoscope · Device: the GlidesScope® Ranger video laryngoscope · Device: the Macintosh laryngoscope

  • Experimental
    Intubation with the GlidesScope® Ranger video laryngoscope

    Participants perform five intubation attempts using the airway manikin with the normal airway setting. After completing the normal airway session, the participants performed another five attempts with the neck immobilization setting using a neck collar.

    Device: the McGrath® MAC video laryngoscope · Device: the GlidesScope® Ranger video laryngoscope · Device: the Macintosh laryngoscope

  • Experimental
    Intubation with Macintosh laryngoscope

    Participants perform five intubation attempts using the airway manikin with the normal airway setting. After completing the normal airway session, the participants performed another five attempts with the neck immobilization setting using a neck collar.

    Device: the McGrath® MAC video laryngoscope · Device: the GlidesScope® Ranger video laryngoscope · Device: the Macintosh laryngoscope

Interventions

  • Devicethe McGrath® MAC video laryngoscope
  • Devicethe GlidesScope® Ranger video laryngoscope
  • Devicethe Macintosh laryngoscope
06

What researchers measure

Primary outcomes

  1. Intubation parameter

    1. The rate for successful intubation 2. Time to intubation 3. The Cormack-Lehane grade at laryngoscopy

    Time frame: 1st intubation attempt, an expected average of 1 min

  2. Intubation parameter

    1. The rate for successful intubation 2. Time to intubation 3. The Cormack-Lehane grade at laryngoscopy

    Time frame: 2nd intubation attempt, an expected average of 1 min

  3. Intubation parameter

    1. The rate for successful intubation 2. Time to intubation 3. The Cormack-Lehane grade at laryngoscopy

    Time frame: 3rd intubation attempt, an expected average of 1 min

  4. Intubation parameter

    1. The rate for successful intubation 2. Time to intubation 3. The Cormack-Lehane grade at laryngoscopy

    Time frame: 4th intubation attempt, an expected average of 1 min

  5. Intubation parameter

    1. The rate for successful intubation 2. Time to intubation 3. The Cormack-Lehane grade at laryngoscopy

    Time frame: 5th intubation attempt, an expected average of 1 min

07

Study locations

1 site
  • Hanyang University Guri Hospital
    Guri-si, Kyeonggi-do 471-701, Korea, Republic of
08

References and documents

Publications

  • Kim W, Choi HJ, Lim T, Kang BS. Can the new McGrath laryngoscope rival the GlideScope Ranger portable video laryngoscope? A randomized manikin study. Am J Emerg Med. 2014 Oct;32(10):1225-9. doi: 10.1016/j.ajem.2014.07.034. Epub 2014 Aug 2. PubMed 25171799 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 31, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02051400
Lead sponsor
Hanyang University
Responsible party
Wonhee Kim (Emergency Medicine Fellow, Department of Emergency Medicine, Hanyang University Seoul Hospital, Hanyang University) — Principal investigator
First posted
Jan 31, 2014
Start date
Sep 2013
Primary completion
Nov 2013
Completion
Nov 2013
Last update
Jan 31, 2014

Study contacts

Hyuk Joong Choi, MD, PhD
study director · Hanyang University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2014. You cannot join it, but the record below documents what was studied.

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