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NCT02289677 Clinical Trial

Pediatric Intubation During CPR

Cardiac Arrest Clinical Trial

— ETICPR  

Official title:
Comparison of the Atmos Scope, the Coopdech and the AirTraq in Pediatric Patients During Resuscitation. Randomized Crossover Manikin Trial

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT02289677
Other study ID # ETI/2014/10
Secondary ID
Status Enrolling by invitation
Phase N/A
First received November 9, 2014
Last updated November 12, 2014
Start date November 2014
Est. completion date November 2014

Study information
Verified date November 2014
Source International Institute of Rescue Research and Education
Contact n/a
Is FDA regulated No
Health authority Poland: Ministry of Science and Higher Education
Study type Interventional

Clinical Trial Summary

We hypothesized that the video-laryngoscopes are beneficial for intubation of pediatric manikins while performing CPR. In the current study, we compared effectiveness of two video-laryngoscopes (the Coopdech video Laryngoscope portable VLp-100 and the Flexible Videoendoscope: ATMOS Scope) and optical-laryngoscope (the AirTraq) during resuscitation with uninterrupted chest compressions using an child manikin.

Recruitment information / eligibility
Status Enrolling by invitation
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 and older
Eligibility Inclusion Criteria:

- Give voluntary consent to participate in the study

- minimum 1 year of work experience in emergency medicine

- experienced emergency medical personnel (physicians, nurses, paramedics)

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:
• ATMOS Scope
Video-laryngoscopy 1
• COOPDECH
Video-laryngoscopy-1
• AirTraq
Optical-laryngoscopy

Locations
Country Name City State
n/a

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

Outcome
Type Measure Description Time frame Safety issue
Primary Success of intubation effectiveness of first, second and third intubation attempts and overall effectiveness of intubation by participants using two intubation devices 1 day No
Secondary Intubation time time in seconds required for a successful intubation attempt 1 day No
Secondary POGO score self-reported percentage of glottis opening (POGO) score 1 day No
Secondary Cormack-Lehane grading self-reported percentage the vocal cord visualization using the Cormack-Lehane grading (grade 1-4) 1 day No
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