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
50 participants
OBSERVATIONAL
2007-04-30
2008-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* contraindication to MRI, contrast agent
* inoperable patients for other reasons
FEMALE
No
Sponsors
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University of Aarhus
OTHER
Principal Investigators
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Liselotte Ibsen, doc
Role: PRINCIPAL_INVESTIGATOR
Aarhus University Hospital, BDA, Skejby
Central Contacts
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Liselotte Ibsen, doc
Role: CONTACT
Other Identifiers
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MR-Center-001
Identifier Type: -
Identifier Source: org_study_id