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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. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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25 April 2016 |
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Main ID: |
NCT02741921 |
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Date of registration:
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13/04/2016 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Conventional Double-lumen Tube vs VivaSight DL
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Scientific title:
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Ability of Anesthesiologist to Placid a Double-lumen Tube. A Randomized Crossover Cadaver Study Comparing VivaSight DL and Conventional Double-lumen Tube |
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Date of first enrolment:
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November 2015 |
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Target sample size:
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27 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02741921 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), 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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Key inclusion & exclusion criteria
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Inclusion Criteria:
- fresh adult cadavers
Exclusion Criteria:
- cadavers with face injures
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Endotracheal Intubation
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Intervention(s)
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Device: conventional double-lumen tube
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Device: VivaSight DL
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Primary Outcome(s)
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Time required for endotracheal intubation
[Time Frame: 1 day]
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Secondary Outcome(s)
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success rate of intubation attempt
[Time Frame: 1 day]
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Time required for visual confirmation of double lumen tube position position
[Time Frame: 1 day]
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Ease of intubation
[Time Frame: 1 day]
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Secondary ID(s)
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02/04/2016
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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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