- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02286323
Endotracheal Intubation During Resuscitation (EIDR)
November 7, 2014 updated by: Lukasz Szarpak, International Institute of Rescue Research and Education
Can the Bonfils Intubation Fiberscope Rival the Macintosh Laryngoscope During Resuscitation With Uninterrupted Chest Compression?
We hypothesized that the BONFILS is beneficial for intubation of manikins while performing CPR.
In the current study we compared the performance of the BONFILS and the Macintosh laryngoscopes with respect to their effectiveness and time to successful ETI during chest compression (CC) using an adult manikin.
Study Overview
Study Type
Interventional
Enrollment (Anticipated)
130
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Masovia
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Warsaw, Masovia, Poland, 04-628
- International Institute of Rescue Research and Education
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Endotracheal intubation without chest compressions
Endotracheal intubation of mannikin during resuscitation without chest compressions.
|
Bonfils Intubation Fiberoscope
Direct laryngoscopy using Macintosh Laryngoscope
|
Experimental: Endotracheal intubation with uninterrupted chest compressions
Endotracheal intubation of mannikin during resuscitation with uninterrupted chest compressions.
In order to simulate the difficulties associated with intubation during uninterrupted chest compressions, CPR was performed by using LUCAS-2 (Physio-Control, Redmond, WA, U.S.).
|
Bonfils Intubation Fiberoscope
Direct laryngoscopy using Macintosh Laryngoscope
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Time to intubation
Time Frame: intraoperative
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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.
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intraoperative
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Success of intubation
Time Frame: intraoperative
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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.
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intraoperative
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POGO score
Time Frame: 1 day
|
self-reported percentage of glottis opening (POGO) score
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1 day
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Andrzej Kurowski, Institute of Cardiology
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2014
Primary Completion (Anticipated)
November 1, 2014
Study Completion (Anticipated)
November 1, 2014
Study Registration Dates
First Submitted
November 5, 2014
First Submitted That Met QC Criteria
November 6, 2014
First Posted (Estimate)
November 7, 2014
Study Record Updates
Last Update Posted (Estimate)
November 10, 2014
Last Update Submitted That Met QC Criteria
November 7, 2014
Last Verified
November 1, 2014
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ETI/2014/07
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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