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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02277951
Other study ID # InternationalIRRE
Secondary ID
Status Completed
Phase N/A
First received October 16, 2014
Last updated October 27, 2014
Start date May 2014
Est. completion date July 2014

Study information

Verified date October 2014
Source International Institute of Rescue Research and Education
Contact n/a
Is FDA regulated No
Health authority Poland: Office for Registration of Medicinal Products, Medical Devices and Biocidal ProductsPoland: The Central Register of Clinical Trials
Study type Observational

Clinical Trial Summary

The aim of the study was to compare time and success rates of four intubation devices ( in a cardiopulmonary scenario with uninterrupted chest compressions with a standardized manikin model.

The investigators hypothesized that fiberoscope laryngoscopes may improve success rates.


Description:

Devices using in study:

The Bonfils Intubation Fibrescope (BONFILS)(KARL STORZ Endovision, Inc., Charlton, MA, USA), The Video Rigid Flexing Laryngoscope (RIFL)( AI Medical Devices, Inc., Williamston, MI, USA), The C-MAC® S Video Laryngoscope Blade Mac#3(C-MAC®S) (KARL STORZ Endovision, Inc., Charlton, MA, USA) The Macintosh Laryngoscope Blade no. 3 (MAC) (LifeLine Medical, Inc., Brooksville, FL, USA).


Recruitment information / eligibility

Status Completed
Enrollment 141
Est. completion date July 2014
Est. primary completion date July 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- experienced emergency personnel: nurses, paramedics

Exclusion Criteria:

- no experience in out-of-hospital emergency medicine

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Device:
The Bonfils Intubation Fibrescope
Effectiveness and time to successful intubation will be measured.
The Video Rigid Flexing Laryngoscope
Effectiveness and time to successful intubation will be measured.
The C-MAC® S Video Laryngoscope
Effectiveness and time to successful intubation will be measured.
The Macintosh Laryngoscope
Effectiveness and time to successful intubation will be measured.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
International Institute of Rescue Research and Education

Outcome

Type Measure Description Time frame Safety issue
Primary Time to successful intubation The devices to be compared include (1) The Bonfils Intubation Fibrescope , (2) the Video Rigid Flexing Laryngoscope, (3) the C-MAC® S Video Laryngoscope, (4) the Macintosh Laryngoscope. Successful intubation will be measured in the seconds from insertion of an intubation device to the first manual ventilation of the mannequin's lungs. Subjects complete study in 1 day No
Primary Success rate of ETI The devices to be compared include (1) The Bonfils Intubation Fibrescope , (2) the Video Rigid Flexing Laryngoscope, (3) the C-MAC® S Video Laryngoscope, (4) the Macintosh Laryngoscope. Successful intubation will be measured in the seconds from insertion of an intubation device to the first manual ventilation of the mannequin's lungs. Subjects complete study in 1 day No
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