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Assessment of Provider Position for Prehospital Tracheal Intubation

Assessment of Provider Position for Prehospital Tracheal Intubation Using Direct Laryngoscopy: Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07165314
Enrollment
72
Registered
2025-09-10
Start date
2023-09-01
Completion date
2024-04-30
Last updated
2025-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tracheal Intubation

Keywords

advanced airway management, laryngoscopy, sitting position, prehospital, manikin, randomized controlled trial

Brief summary

Endotracheal intubation may be needed in critically ill patients in the prehospital setting, where difficult conditions may be encountered. The patient may be lying on the ground, thus complicating direct laryngoscopy as the operator's visual axis cannot be properly aligned with the patient's oral-pharyngeal-tracheal axis. The posture sitting cross-legged (Lotus position) at the head of the patient may allow an easier alignment of the visual axes due to a lower operator's head position and more stability. We compared the impact of the Lotus position with free positioning of the operator for direct laryngoscopy on intubation first pass success rate among novice operators.

Interventions

PROCEDUREFree positioning

Participants are not given instructions on how to position for intubation using direct laryngoscopy.

PROCEDURESitting cross-legged (Lotus position)

Participants are requested to sit cross-legged for intubation using direct laryngoscopy.

Sponsors

University Hospital, Geneva
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* All resident doctors 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 take part in the research

Exclusion criteria

* More than 6 years of post-graduate experience * Performed more than 10 ETIs prior to take part in the research

Design outcomes

Primary

MeasureTime frameDescription
First Pass Success ratePeriproceduralIn percentage, defined as achieving successful ETI on the initial attempt. An ETI attempt was counted since the laryngoscope blade was inserted at the dental arch, regardless of whether tracheal tube placement was attempted or not. ETI was considered successful when adequate ventilation was confirmed by chest elevation. The number of intubation attempts were limited to three, with a time limit of 60 seconds allowed per attempt.

Secondary

MeasureTime frameDescription
Time to Intubation for the first intubation attempt alonePeriproceduralTime in seconds from blade insertion at the dental arch to adequate ventilation, ruling out first-attempt failures. A maximum of 60 seconds was allowed per ETI attempt.
Number of intubations attemptsPeriproceduralAn ETI attempt was counted since the laryngoscope blade was inserted at the dental arch, regardless of whether tracheal tube placement was attempted or not. ETI was considered successful when adequate ventilation was confirmed by chest elevation. The number of intubation attempts were limited to three, with a time limit of 60 seconds allowed per attempt.
Time to IntubationPeriproceduralTime in seconds from blade insertion at the dental arch to successful ventilation. A maximum of 60 seconds was allowed per ETI attempt.
Percentage Of Glottis Opening (POGO) scorePeriproceduralFor each attempt, the percentage of glottis opening was assessed by the participant, using the POGO score.
Subjective assessmentsPeriproceduralPerceived difficulty was appraised using a 5-point Likert scale ranging from Totally Agree to Totally Disagree.
Cormack and Lehane (CL) scorePeriproceduralFor each attempt, the view of the larynx was assessed by the participant using the Cormack-Lehane score.

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026