Double Lumen Tube Intubation
- Conditions
- Cardiac ArrestEndotracheal Intubation
- Interventions
- Device: standard double-lumen tubeDevice: VivaSight Double Lumen Tube
- Registration Number
- NCT02295657
- Lead Sponsor
- International Institute of Rescue Research and Education
- Brief Summary
The aim of this study was to compare time, success rates of different double-lumen tubes in intubation in a standardized manikin model.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 120
- give voluntary consent to participate in the study
- minimum 1 year of work experience in emergency medicine
- experienced emergency medicine personnel (physicians, nurses, paramedics)
- not meet the above criteria
- wrist or low back diseases
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description ETI intubation VivaSight Double Lumen Tube endotracheal intubation in manikin ETI intubation standard double-lumen tube endotracheal intubation in manikin
- Primary Outcome Measures
Name Time Method Success of intubation 1 day effectiveness of first, second and third intubation attempts and overall effectiveness of intubation by participants
- Secondary Outcome Measures
Name Time Method Cormack-Lehane grading 1 day self-reported percentage the vocal cord visualization using the Cormack-Lehane grading (grade 1-4)
Intubation time 1 day time in seconds required for a successful intubation attempt
Preferred ETI device 1day participants were asked which method of ETI they would prefer in a real-life.
Trial Locations
- Locations (1)
International Institute of Rescue Research and Education
🇵🇱Warsaw, Masovia, Poland