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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02277418
Other study ID # ETI/2014/05
Secondary ID
Status Completed
Phase N/A
First received October 27, 2014
Last updated November 13, 2014
Start date October 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

The purpose of this study was to compare the Venner a.p. advance video laryngoscope to Miller laryngoscope during resuscitation with and without chest compressions.


Description:

Endotracheal intubation (ETI) is a life-saving procedure performed daily in emergency medicine. The European Resuscitation Council (ERC) 2010 cardiopulmonary resuscitation (CPR) guidelines suggest that intubators should be able to secure the airway without interrupting chest compression. However, ETI with uninterrupted chest compression in patients can be a very difficult skill to acquire.


Recruitment information / eligibility

Status Completed
Enrollment 112
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 (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:
VAVL
Videolaryngoscope
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 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 POGO score self-reported percentage of glottis opening (POGO) score 1 day No
Secondary VAS score participants were asked which method they would prefer in a real-life resuscitation. 1 day No
Secondary Cormack-Lehan scale self reported Cormack-Lehan scale during intubation 1 day No
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