Intubation During Pediatric Resuscitation
- Conditions
- Pediatric ManikinEndotracheal IntubationCardiac Arrest
- Registration Number
- NCT02277015
- Lead Sponsor
- International Institute of Rescue Research and Education
- Brief Summary
The European Resuscitation Council (ERC) 2010 cardiopulmonary resuscitation (CPR) guidelines suggest that intubators should be able to secure the airway without interrupting chest compression. We examine the performance of the Berci-Kaplan DCI (BERCI), the GlideScope (GVL), the AirTraq, the Pentax AWS (Pentax) and the Miller laryngoscope (MIL) for endotracheal intubation (ETI) during pediatric resuscitation with and without chest compressions.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 94
- 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
- Primary Outcome Measures
Name Time Method Intubation Time 1 month time in seconds required for a successful intubation attempt with the five different ETI devices
- Secondary Outcome Measures
Name Time Method Overall Success intraoperative Overall success rate will be defined as the total number of successful placements divided by the total number of patients treated.
Successful intubation 1 month effectiveness of first, second, third intubation attempts and overall effectiveness intubation attempt using all intubation devices
First Pass Attempt 1 month Endotracheal Intubation (ETI) attempt will be defined as tip of the laryngoscope blade passing the patient's lips. First attempt success rate will be defined as the number of successful placements occurring on the first attempt to place the endotracheal tube.
POGO score 1 month self reported percentage og glottis opening (POGO) score
VAS score 1 month To assess subjective opinion about the difficulty of the procedure, participants were asked to rate it on a visual analogue scale (VAS) with a score from 1 (very easy) to 5 (very difficult).
Preferred ETI device 1 month 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