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Comparison of the Vividtrac™ and Other Videolaryngoscopes in Clinical Practice

U

University of Pecs

Status

Unknown

Conditions

Intubation;Difficult

Treatments

Device: Vividtrac videolaryngoscope
Device: KingVision videolaryngoscope
Device: Direct laryngoscopy

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Comparison of various videolaryngoscope devices (Vividtrac™ and KingVision™) and direct laryngoscopy with Macintosh blade regarding laryngoscopy time, intubation time, intubation success rate, percentage of visible glottic opening (POGO score) in elective and acute clinical anaesthesiology practice.

Enrollment

150 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • written informed consent
  • over 18 years of age
  • elective intervention
  • no anticipated difficult airway or intubation
  • preoperative anaesthesia risk assessment by American Society of Anaesthesiologists (ASA) physical status classification: ASA grade I-II

Exclusion criteria

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

150 participants in 3 patient groups

Macintosh laryngoscopy
Active Comparator group
Description:
In this group intubation attempt is carried out with a standard Macintosh (size 3 or 4) direct laryngoscopy blade.
Treatment:
Device: Direct laryngoscopy
KingVision videolaryngoscope
Active Comparator group
Description:
In this group intubation attempt is carried out with KingVision videolaryngoscope with a channeled, disposable single-use blade.
Treatment:
Device: KingVision videolaryngoscope
VividTrac videolaryngoscope
Active Comparator group
Description:
In this group intubation attempt is carried out with VividTrac Adult model using a smartphone or laptop running the VividVision proprietary software.
Treatment:
Device: Vividtrac videolaryngoscope

Trial contacts and locations

1

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Central trial contact

Gábor Woth, MD PhD; Dóra Keresztes, MD

Data sourced from clinicaltrials.gov

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