Pediatric Intubation Among Nursing

Cardiac Arrest Clinical Trial

Official title:

Coparison of Miller and CoPilot Laryngoscopes for Intubation by Nurses During Child Chest Compression. A Manikin Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02291640
• Other study ID #: ETI/2014/16
• Status: Recruiting
• Phase: N/A
• First received: November 11, 2014
• Last updated: November 11, 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 aim of this study was to compare time, success rates of video laryngoscope and direct laryngoscope for the emergency intubation with an immobilized cervical spine in a standardized pediatric manikin model.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 130
• Est. completion date: December 2014
• Est. primary completion date: December 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

• Cardiac Arrest
• Heart Arrest
• Intubation, Endotracheal

Intervention

Device:
• MIL
direct laryngoscopy
• CoPilot
video 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
Other	Cormack-Lehan scale	self reported Cormack-Lehan scale during intubation	1 day	No
Primary	Success of intubation	effectiveness of the first, second and third intubation attempts and overall effectiveness of intubation by participants using four intubation devices.	1 day	No
Secondary	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.If the examinee failed at all attempts, the case was excluded from the time calculations.	1 day	No