Prospective Observation for Serial Changes of Acute Intracranial Artery Dissection Using High Resolution MRI
NCT ID: NCT02914288
Last Updated: 2016-09-26
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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UNKNOWN
20 participants
OBSERVATIONAL
2016-04-30
2018-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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High resolution magnetic resonance imaging for intracranial vessel walls
High resolution magnetic resonance imaging for intracranial vessel walls at initial (optional), 1 month, 3 month, 6 month (optional), and 12 month
Eligibility Criteria
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Inclusion Criteria
* acute intracranial artery dissection
Exclusion Criteria
* contraindication for MR imaging,
* Hypersensitivity to gadolinium based contrast media,
* Pregnant or lactating women,
* Renal condition : eGFR \< 60, 6) Patients unable and/or unwilling to comply with treatment or study instructions
ALL
No
Sponsors
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Ministry of Health & Welfare, Korea
OTHER_GOV
Bracco Corporate
INDUSTRY
Asan Medical Center
OTHER
Responsible Party
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Seung Chai Jung
MD. PhD.
Principal Investigators
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Seung Chai Jung, MD.,PhD.
Role: PRINCIPAL_INVESTIGATOR
Asan Medical Center
Locations
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Asan Medical Center
Seoul, Seoul, South Korea
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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ICD_02
Identifier Type: -
Identifier Source: org_study_id
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