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NCT02293226 Clinical Trial

Video-laryngoscopy During Chest Compression

Cardiac Arrest Clinical Trial

— VIDEO  

Official title:
Comparison of Four Video-laryngoscopes During Pediatric Intubation During Simulated Resuscitation

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT02293226
Other study ID # ETI/2014/19
Secondary ID
Status Not yet recruiting
Phase N/A
First received November 13, 2014
Last updated November 17, 2014
Start date November 2014
Est. completion date December 2014

Study information
Verified date November 2014
Source International Institute of Rescue Research and Education
Contact Andrzej Kurowski
Phone +48500186225
Email andrzejkurowski987@gmail.com
Is FDA regulated No
Health authority Poland: Ministry of Science and Higher Education
Study type Interventional

Clinical Trial Summary

The investigators will compare the success rates and time to successful intubation of endotracheal intubation during simulated pediatric and infant resuscitation with and without chest compression using four different video-laryngoscopes.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 150
Est. completion date December 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

- Minimum 1 year of work experience in nursing

Exclusion Criteria:

- Not meet the above criteria

- Wrist or low back diseases

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Device:
• CoopDech
Video-laryngoscopy 1
• CoPilot
video-laryngoscopy 2
• Intubrite
Video-laryngoscopy 3
• Vividtrack
video-laryngoscopy 4

Locations
Country Name City State
Poland International Institute of Rescue Research and Education Warsaw Masovia

Sponsors (1)
Lead Sponsor Collaborator
International Institute of Rescue Research and Education

Country where clinical trial is conducted

Poland, 

Outcome
Type Measure Description Time frame Safety issue
Primary Time to intubation time from insertion of the blade to the first manual ventilation of the manikin´s lungs. If time of intubation is over than 60 seconds, attempt was recognized as failure. 1 day 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. 1 day No
Secondary Cormack-Lehan scale self reported Cormack-Lehan scale during intubation 1 day No
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