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Evaluation of Airway Adjuncts for Intubation in Entrapped Patients With Difficult Airway Access

NCT06609499 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2025-09-05

No results posted yet for this study

Summary

The aim of this clinical trial is to evaluate two airway adjuncts for intubation in a simulated condition of an entrapped trauma patient with simultaneous cervical spine immobilisation. All the studied devices are evaluated by fully-qualified and experienced paramedics (both male and female). The main questions it aims to answer are:

Which device requires the shortest time required to achieve a successful intubation and ventilation? What is the first attempt success rate of the studied devices? Which device is the easiest to use and the most user-friendly? Study participants will evaluate two different airway adjuncts for intubation in a restricted access to the entrapped trauma patient's airway. The maximum number of insertion attempts is limited to three per device.

Conditions

  • Airway Obstruction

Interventions

DEVICE

Flexible-tip Bougie

The device is used for intubation and then the manikin is ventilated

DEVICE

Gum-elastic Bougie

The device is used for intubation and then the manikin is ventilated

Sponsors & Collaborators

  • Uniwersytet Radomski im. Kazimierza Pułaskiego

    lead OTHER

Principal Investigators

  • Dawid J Aleksandrowicz, PhD · University of Radom

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
25 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-03-15
Primary Completion
2025-05-01
Completion
2025-05-31

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06609499 on ClinicalTrials.gov