Evaluating airway devices for intubation in trapped trauma patients
Standard Gum Elastic Bougie Versus Flexible-tip Bougie: Evaluation of Airway Adjuncts for Intubation in Entrapped Patients With Difficult Airway Access - a Randomised, Controlled Trial
This study tests two different airway devices to see which one helps paramedics intubate trapped trauma patients more quickly and easily.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 25 Years to 55 Years |
| Sex | All |
| Sponsor | Uniwersytet Radomski im. Kazimierza Pułaskiego Academic / other |
| Locations | 1 site (Radom, Mazowieckie) |
| Trial ID | NCT06609499 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates two airway adjuncts for intubation in a simulated scenario involving an entrapped trauma patient with cervical spine immobilization. Qualified paramedics will assess the devices based on the time taken for successful intubation, first attempt success rates, and user-friendliness. Participants will undergo a brief training session before practicing on a manikin secured in a vehicle, with limited access to the airway. The study aims to determine which device is more effective under challenging conditions.
Who should consider this trial
Good fit: Ideal candidates for this study are fully-qualified paramedics with at least four years of experience.
Not a fit: Paramedics in training or retired paramedics will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve intubation outcomes for trauma patients with difficult airway access.
How similar studies have performed: While similar studies have been conducted, this specific evaluation of airway adjuncts in a simulated entrapped scenario is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * fully-qualified paramedics * at least four years of practice after finishing paramedic training * active (working) paramedics Exclusion Criteria: * paramedics in training * retired paramedics * lack of written informed consent
Where this trial is running
Radom, Mazowieckie
- University of Radom — Radom, Mazowieckie, Poland (Recruiting)
Study contacts
- Principal investigator: Dawid J Aleksandrowicz, PhD — University of Radom
- Study coordinator: Dawid J Aleksandrowicz, PhD
- Email: d.aleksandrowicz@urad.edu.pl
- Phone: +48483617350
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.