NCT06918717

Brief Summary

Tracheal intubation using videolaryngoscopy may be required in the prehospital setting, where airway management presents unique technical and logistical challenges. Intubation may be hard because novice providers performing videolaryngoscopy may only look at the screen and only obtain a two-dimensional representation of the patient's airways. By directly visualizing the airways, these providers may obtain a better 3D apprehension and an improved mental visualization of the patient's anatomy. We aim to compare the impact of a freely realized videolaryngoscopy sequence with a sequence consisting in direct visualization of the airway followed by videolaryngoscopy ("Direct Laryngoscopy-to-VideoLaryngoscopy sequence" or "DL-VL sequence") on time to intubation among novice providers.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
72

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 10, 2023

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 20, 2024

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 15, 2024

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

March 26, 2025

Completed
14 days until next milestone

First Posted

Study publicly available on registry

April 9, 2025

Completed
Last Updated

April 9, 2025

Status Verified

April 1, 2025

Enrollment Period

7 months

First QC Date

March 26, 2025

Last Update Submit

April 1, 2025

Conditions

Keywords

Advanced airway managementdirect laryngoscopytracheal intubationprehospitalvideolaryngoscopy

Outcome Measures

Primary Outcomes (1)

  • Time to Intubation

    Time in seconds from blade insertion at the dental arch to adequate tracheal tube placement through the vocal cords, confirmed by the C-MAC video recording. A maximum of 60 seconds was allowed per ETI attempt. The maximum number of ETI attempts was limited to 3.

    Periprocedural

Secondary Outcomes (5)

  • Time to Intubation for the first intubation attempt alone

    Periprocedural

  • First Pass Success rate

    Periprocedural

  • Number of intubations attempts

    Periprocedural

  • Time to Ventilation

    Periprocedural

  • Subjective assessments

    Periprocedural

Study Arms (2)

Free use of videolaryngoscopy

ACTIVE COMPARATOR
Procedure: Free use of videolaryngoscopy

Direct Laryngoscopy-to-VideoLaryngoscopy sequence

EXPERIMENTAL
Procedure: Direct Laryngoscopy-to-VideoLaryngoscopy sequence

Interventions

Participants will proceed with a double intubation technique sequence, first performing an initial direct laryngoscopy without looking at the video screen until they reached the epiglottis, then performing an indirect lryngoscopy for intubation.

Direct Laryngoscopy-to-VideoLaryngoscopy sequence

Participants are free to use of the videolaryngoscope as they intended

Free use of videolaryngoscopy

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • All resident physicians with 1 to 6 years of post-graduate experience working in the Emergency Department (ED) at Geneva University Hospitals (Hôpitaux Universitaires de Genève (HUG)) and penultimate year of medical school students (5th year) studying at University of Geneva Faculty of Medicine (UGFM).
  • Performed less than 10 ETIs prior to participating in the study.

You may not qualify if:

  • More than 6 years of post-graduate experience
  • Performed more than 10 ETIs prior to participating in the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hôpitaux Universitaires de Genève

Geneva, Canton of Geneva, 1205, Switzerland

Location

Related Publications (1)

  • Cibotto C, Pasquier M, Beysard N, Rouyer F, Grosgurin O, Bourgeois L, Erriquez E, Braun E, Gartner BA, Desmettre T, Suppan L. Assessment of prehospital tracheal intubation technique using initial direct laryngoscopy during videolaryngoscopy: randomized controlled simulated trial. BMC Emerg Med. 2025 Jul 1;25(1):112. doi: 10.1186/s12873-025-01266-0.

Study Officials

  • PD Dr Laurent Suppan

    University Hospital, Geneva

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

March 26, 2025

First Posted

April 9, 2025

Study Start

September 10, 2023

Primary Completion

April 20, 2024

Study Completion

August 15, 2024

Last Updated

April 9, 2025

Record last verified: 2025-04

Locations