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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02286297
Other study ID # ETI/2014/08
Secondary ID
Status Recruiting
Phase N/A
First received November 5, 2014
Last updated November 6, 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 Lukasz Czyzewski
Email rn.czyzewski@gmail.com
Is FDA regulated No
Health authority Poland: Ministry of Science and Higher Education
Study type Interventional

Clinical Trial Summary

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.


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

- paramedics, nurses, physicians

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:
McGRATH® MAC
video-laryngoscopy-1
AirTraq
video-laryngoscopy-2
GlideScope
video-laryngoscopy-3
Miller
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 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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