Survey of Current Interventional and Diagnostic Imaging Residents After Participation in Endovascular Simulator Training
NCT ID: NCT04832698
Last Updated: 2025-11-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
9 participants
OBSERVATIONAL
2020-07-08
2026-04-30
Brief Summary
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Detailed Description
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I. To measure trainee comfort performing simulated endovascular procedures after completing training on the Mentice endovascular simulator device.
OUTLINE:
Participants complete a survey over 10 minutes before and after completing training and using the Mentice endovascular simulator device.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Observational (survey administration)
Participants complete a survey over 10 minutes before and after completing training and using the Mentice endovascular simulator device.
Survey Administration
Complete survey
Interventions
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Survey Administration
Complete survey
Eligibility Criteria
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Inclusion Criteria
18 Years
ALL
Yes
Sponsors
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National Cancer Institute (NCI)
NIH
M.D. Anderson Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Joshua D Kuban
Role: PRINCIPAL_INVESTIGATOR
M.D. Anderson Cancer Center
Locations
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M D Anderson Cancer Center
Houston, Texas, United States
Countries
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Central Contacts
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Facility Contacts
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Related Links
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MD Anderson Cancer Center Website
Other Identifiers
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NCI-2020-06610
Identifier Type: REGISTRY
Identifier Source: secondary_id
2020-0071
Identifier Type: OTHER
Identifier Source: secondary_id
2020-0071
Identifier Type: -
Identifier Source: org_study_id
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