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Teleguidance-facilitated Airway Management

Remote Teleguidance-facilitated Airway Management in Prehospital Emergency Medical Services: A Randomized Controlled Simulation Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06497725
Enrollment
98
Registered
2024-07-12
Start date
2024-05-01
Completion date
2024-08-01
Last updated
2024-08-14

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

Conditions

Emergencies, Intubation; Difficult or Failed, Telemedicine

Brief summary

The advent of telemedicine has introduced teleguidance as a promising support to enhance endotracheal intubation skills among inexperienced operators. Several studies showed the effectiveness of supervisor assisted ETI using the various VL devices and commercial videoconferencing softwares. However, recent developments in VL technologies introduced the VL integrated videoconferencing features for this purpose. Scoper VL device (Technomedicare Inc, Turkiye) developed a real-time teleconsultation feature for difficult airway scenarios to be assisted by experts during the procedure. However, the literature is very limited about the effectiveness and feasibility of teleguidance-facilitated airway management. This high-fidelity simulation study aims to assess impact of teleguidance-facilitated airway management on the success of ETI performed by inexperienced operators in a mobile ambulance.

Interventions

DEVICETeleguidance-facilitated Airway Management

tele-guidence will be provided by an experienced airway expert

Sponsors

Kocaeli University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* All paramedic students who completed their airway management training

Exclusion criteria

* The trainees who did not consent to participate * The trainees who did not complete the VL training

Design outcomes

Primary

MeasureTime frameDescription
Rate of first attempt success (n,%)Measured at the 60-second mark.Visualization of the endotracheal tube passing between the vocal cords within the first 60 seconds of the procedure.

Secondary

MeasureTime frameDescription
Intubation duration (seconds)procedure (Measured at the confirmation of the tube passed between vocal cords.)Duration between the passage of the endotracheal tube through the lips and its pass between the vocal cords
Operator confidence assessed by Likert Scale.At the end of the procedureSelf-evaluation of procedure confidence using 7-point Likert Scale
Feasibility of intubation assessed by Likert Scale.At the end of the procedureSelf-evaluation of methods feasibility using 7-point Likert Scale

Countries

Turkey (Türkiye)

Outcome results

None listed

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