Prehospital Tracheal Intubation Technique Using Initial Direct Laryngoscopy During Videolaryngoscopy
Assessment of Prehospital Tracheal Intubation Technique Using Initial Direct Laryngoscopy During Videolaryngoscopy: Randomized Controlled Simulated Trial
1 other identifier
interventional
72
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Sep 2023
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 10, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 20, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 15, 2024
CompletedFirst Submitted
Initial submission to the registry
March 26, 2025
CompletedFirst Posted
Study publicly available on registry
April 9, 2025
CompletedApril 9, 2025
April 1, 2025
7 months
March 26, 2025
April 1, 2025
Conditions
Keywords
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 COMPARATORDirect Laryngoscopy-to-VideoLaryngoscopy sequence
EXPERIMENTALInterventions
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.
Participants are free to use of the videolaryngoscope as they intended
Eligibility Criteria
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
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.
PMID: 40596822DERIVED
Study Officials
- STUDY DIRECTOR
PD Dr Laurent Suppan
University Hospital, Geneva
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