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NCT02289638 Clinical Trial

Effectiveness of Child Intubation

Cardiac Arrest Clinical Trial

Official title:
First Comparison of the /Intubrite VideoLaryngoscope System Versus the Miller Laryngoscope for Intubations by Non-anaesthetists: a Manikin Study.

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02289638
Other study ID # ETI/2014/13
Secondary ID
Status Recruiting
Phase N/A
First received November 10, 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 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

We hypothesized that the Intubrite Video Laryngoscope System VLS 6600 is beneficial for intubation of pediatric manikins while performing CPR. In the current study, we compared effectiveness of the Intubrite and MIL laryngoscopes in child resuscitation with and without CC.

Recruitment information / eligibility
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

- 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:
• Intubrite
Video-Laryngoscopy
• MIL
Direct-Laryngoscopy

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 Success of intubation effectiveness of first, second and third intubation attempts and overall effectiveness of intubation by participants 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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