Direct Laryngoscopy During Cervical Trauma
Not Applicable
- Conditions
- Trauma
- Registration Number
- NCT02292693
- Lead Sponsor
- International Institute of Rescue Research and Education
- Brief Summary
The aim of this study was to compare time, success rates of different laryngoscope blades for intubation with an immobilized cervical spine in a standardized pediatric manikin model.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
- give voluntary consent to participate in the study
- minimum 1 year of work experience in emergency medicine
- experienced emergency medicine personnel (physicians, nurses, paramedics)
Exclusion Criteria
- not meet the above criteria
- wrist or low back diseases
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- 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 Intubation time 1 day time in seconds required for a successful intubation attempt
Cormack-Lehane grading 1 day self-reported percentage the vocal cord visualization using the Cormack-Lehane grading (grade 1-4)
Preferred ETI device 1day participants were asked which method of ETI they would prefer in a real-life resuscitation.
Trial Locations
- Locations (1)
International Institute of Rescue Research and Education
🇵🇱Warsaw, Masovia, Poland
International Institute of Rescue Research and Education🇵🇱Warsaw, Masovia, Poland