Pediatric Clinical Trial
— PETIOfficial title:
Comparison of Intubation Through the McGrath® MAC, GlideScope®, AirTraq® and Miller Laryngoscope by Paramedics During Pediatric Cardiopulmonary Resuscitation: a Randomized Crossover Manikin Trial.
Endotracheal intubation (ETI) is perceived as the optimal method of providing and maintaining a clear and secure airway. The 2010 European Resuscitation Council (ERC) guidelines emphasized the importance of minimal interruption during cardiopulmonary resuscitation (CPR). These guidelines also suggest that skilled operators should be able to secure the airway without interrupting chest compression. The aim of the study was to compare time and success rates of different available video laryngoscopes and the Miller laryngoscope for emergency intubation during simulated pediatric CPR.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | November 2014 |
Est. primary completion date | November 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - give voluntary consent to participate in the study - paramedics, nurses, physicians Exclusion Criteria: - not meet the above criteria - wrist or low back diseases |
Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Poland | International Institute of Rescue Research and Education | Warsaw | Masovia |
Lead Sponsor | Collaborator |
---|---|
International Institute of Rescue Research and Education |
Poland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Time to intubation | time from insertion of the blade to the first manual ventilation of the manikinĀ“s lungs. If time of intubation is over than 60 seconds, attempt was recognized as failure. | intraoperative | No |
Secondary | Success of intubation | effectiveness of the first, second and third intubation attempts and overall effectiveness of intubation by participants using four intubation devices. If the examinee failed at all attempts, the case was excluded from the time calculations. | intraoperative | No |
Secondary | Visual Analog scale (VAS) score | participants were asked which method they would prefer in a real-life resuscitation | 1 day | No |
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