Endotracheal Intubation Devices

Intubation Clinical Trial

— ETID  

Official title:

Comparison of Four Different Endotracheal Intubation Devices Performed by Emergency Medical Professionals: a Manikin Study With 6 Airway Scenarios

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02277652
• Other study ID #: ETI/2014/03
• Status: Recruiting
• Phase: N/A
• First received: October 26, 2014
• Last updated: November 11, 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: Lukasz Szarpak
• Phone: (+48)500186225
• Email: lukasz.szarpak[@]gmail.com
• 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 four different intubation devices in 6 different scenarios.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 120
• 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 (paramedics, nurses, physicians)

Exclusion Criteria:

• not meet the above criteria

• wrist or low back diseases

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Intubation

Intervention

Device:
• The Miller Laryngoscope
Direct laryngoscopy
• The Bonfils intubation fibrescope
Optical laryngoscopy
• The GlideScope Ranger
Videolaryngoscopy
• The Supraglottic Airway Laryngopharyngeal Tube (SALT)
Blind intubation

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 month	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 month	No
Secondary	POGO score	self-reported percentage of glottis opening (POGO) score	1 month	No
Secondary	VAS score	participants were asked which method they would prefer in a real-life resuscitation.	1 month	No
Secondary	Cormack-Lehane grading	self-reported percentage the vocal cord visualization using the Cormack-Lehane grading (grade 1-4)	1 month	No