Clopidogrel Response in Acute Ischemic Stroke. The Bochumer CRISP Study
NCT ID: NCT01843361
Last Updated: 2013-04-30
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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COMPLETED
159 participants
OBSERVATIONAL
2010-07-31
2012-12-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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acute ischemic stroke
Determing cardiovascular risk factors or medication on clopidogrel response rates after an acute ischemic stroke
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* admittance to stroke unit
* clopidogrel medication
Exclusion Criteria
* prior bleeding disorders
* severe liver disorders
* current gastrointestinal disorders
* congestive heart failure
* life-threatening malignancies
18 Years
ALL
No
Sponsors
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Ruhr University of Bochum
OTHER
Responsible Party
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Saskia Meves
MD
Principal Investigators
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Saskia H Meves, MD
Role: PRINCIPAL_INVESTIGATOR
Ruhr University Bochum, Department of Neurology
Locations
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Department of Neurology, Ruhr University Bochum
Bochum, , Germany
Countries
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References
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Meves SH, Overbeck U, Endres HG, Krogias C, Neubauer H. Dose-dependent effect of early antiplatelet therapy in acute ischaemic stroke. Thromb Haemost. 2012 Jan;107(1):69-79. doi: 10.1160/TH11-06-0436. Epub 2011 Dec 8.
Fong J, Cheng-Ching E, Hussain MS, Katzan I, Gupta R. Predictors of biochemical aspirin and clopidogrel resistance in patients with ischemic stroke. J Stroke Cerebrovasc Dis. 2011 May-Jun;20(3):227-30. doi: 10.1016/j.jstrokecerebrovasdis.2009.12.004. Epub 2010 Jul 10.
Other Identifiers
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Meves-clopi-01
Identifier Type: -
Identifier Source: org_study_id