Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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19 February 2015 |
Main ID: |
NCT02295657 |
Date of registration:
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18/11/2014 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Double Lumen Tube Intubation
DLETI |
Scientific title:
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Comparison of Techniques for Double-lumen Tube Intubation: Standard Double-lumen Tube or VivaSight Double Lumen Tube by Paramedics. A Randomized Crossover Manikin Trial. |
Date of first enrolment:
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November 2014 |
Target sample size:
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120 |
Recruitment status: |
Recruiting |
URL:
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http://clinicaltrials.gov/show/NCT02295657 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Poland
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Contacts
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Name:
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Lukasz Szarpak |
Address:
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Telephone:
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+48500186225 |
Email:
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lukasz.szarpak@gmail.com |
Affiliation:
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Name:
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Andrzej Kurowski |
Address:
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Telephone:
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+48500186225 |
Email:
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andrzejkurowski987@gmail.com |
Affiliation:
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Name:
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Lukasz Szarpak |
Address:
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Telephone:
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Email:
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Affiliation:
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Institute of Cardiology |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- give voluntary consent to participate in the study
- minimum 1 year of work experience in emergency medicine
- experienced emergency medicine personnel (physicians, nurses, paramedics)
Exclusion Criteria:
- not meet the above criteria
- wrist or low back diseases
Age minimum:
18 Years
Age maximum:
65 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Cardiac Arrest
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Endotracheal Intubation
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Intervention(s)
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Device: standard double-lumen tube
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Device: VivaSight Double Lumen Tube
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Primary Outcome(s)
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Success of intubation
[Time Frame: 1 day]
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Secondary Outcome(s)
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Cormack-Lehane grading
[Time Frame: 1 day]
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Intubation time
[Time Frame: 1 day]
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Preferred ETI device
[Time Frame: 1day]
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Secondary ID(s)
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ETI/2014/43
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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