CClinicalTrials.gg
CompletedNCT02344030KingVisionUpdated Aug 3, 2018

Comparsion of King Vision® Standard Blade and King Vision® Channeled Blade in Patients Scheduled for Tracheal Intubation

An interventional study of channeled blade and standard blade in Hypoxemia, sponsored by Johannes Gutenberg University Mainz. Completed at 1 site in Germany. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2018-08-03.

Sponsored by Johannes Gutenberg University Mainz · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
44
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Comparison of intubation time from the time to fix the Trachealtube to the first end-tidal CO2 ventilation by means of the curve on the ventilator at KV standard blade and KV channeled blade

Read the detailed description

In the proposed clinical trial the time measured until the first manual ventilation at 44 study participants with elective anesthesia by using the KV standard blade and KV channeled blade. Bedside the time for tracheal intubation, we documented the view on the monitor which is connected to the instrument, the C\& L classification and POGO Scale.

02

Conditions studied

  • Hypoxemia

Browse trials for

Keywords

  • airway
  • videolaryngoscope
03

In context

Hypoxia

1,231 studies on the registry are indexed under Hypoxia; 241 are open to participants now.

This study's enrollment of 44 is close to the median of 45 across 853 interventional studies indexed under Hypoxia.

Browse Hypoxia studies →

Lead sponsor

Johannes Gutenberg University Mainz is the lead sponsor of 153 studies on the registry; 20 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age ≥ 18 Years No concurrent participation in another study
  • capacity to consent
  • Present written informed consent of the research participant
  • Elective surgery under general anesthesia

Exclusion criteria

Exclusion Criteria:

  • Age \<18 years
  • Existing pregnancy
  • Lack of consent
  • inability to consent
  • emergency patients
  • Emergency situations in the context of a Difficult Airway Management
  • ASA classification> 3
  • situations where the possibility of accumulated gastric contents
  • Participation in another study
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
44 participants (actual)

Study arms

  • Experimental
    standard blade

    Standard Blade: tracheal intubation with standard blade

    Device: channeled blade · Device: standard blade

  • Experimental
    channeled blade

    Channeled Blade: tracheal intubation with channeled blade

    Device: channeled blade · Device: standard blade

Interventions

  • Devicechanneled blade

    In a randomised trial we measure the time for ventilation by means of endtidale CO2 Curve

  • Devicestandard blade

    In a randomised trial we measure the time for ventilation by means of endtidale CO2 Curve

06

What researchers measure

Primary outcomes

  1. comparison of different time for tracheal intubation

    We want to measure the time for tracheal intubation

    Time frame: <2min

07

Study locations

1 site
  • Department of Anesthesiology,Prof. C. Werner, Universitätsmedizin of the JG University
    Mainz, Rhineland-Palatinate D55131, Germany
08

References and documents

Publications

  • Murphy LD, Kovacs GJ, Reardon PM, Law JA. Comparison of the king vision video laryngoscope with the macintosh laryngoscope. J Emerg Med. 2014 Aug;47(2):239-46. doi: 10.1016/j.jemermed.2014.02.008. Epub 2014 Apr 16. PubMed 24742495 ↗
  • Akihisa Y, Maruyama K, Koyama Y, Yamada R, Ogura A, Andoh T. Comparison of intubation performance between the King Vision and Macintosh laryngoscopes in novice personnel: a randomized, crossover manikin study. J Anesth. 2014 Feb;28(1):51-7. doi: 10.1007/s00540-013-1666-9. Epub 2013 Jun 30. PubMed 23812581 ↗
  • Kriege M, Alflen C, Noppens RR. Using King Vision video laryngoscope with a channeled blade prolongs time for tracheal intubation in different training levels, compared to non-channeled blade. PLoS One. 2017 Aug 31;12(8):e0183382. doi: 10.1371/journal.pone.0183382. eCollection 2017. PubMed 28859114 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 3, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02344030
Lead sponsor
Johannes Gutenberg University Mainz
Responsible party
Marc Kriege, MD (Marc Kriege, MD, Johannes Gutenberg University Mainz) — Principal investigator
First posted
Jan 22, 2015
Start date
Jan 2015
Primary completion
Feb 2015
Completion
Feb 2015
Last update
Aug 3, 2018

Study contacts

Marc Kriege, MD
principal investigator · University JG, Mainz

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2018. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion