Clopidogrel Response in Acute Ischemic Stroke

NCT ID: NCT01846572

Last Updated: 2013-05-03

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

159 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-07-31

Study Completion Date

2012-12-31

Brief Summary

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The aim of this study was to determine the prevalence rate and risk factors for chemical laboratory clopidogrel low-response (CLR) in the acute phase after an ischemic stroke.

Detailed Description

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Conditions

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Ischemic Stroke

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* acute ischemic stroke
* admittance to stroke unit
* clopidogrel medication

Exclusion Criteria

* no consent
* prior bleeding disorders
* severe liver disorders
* current gastrointestinal disorders
* congestive heart failure
* life-threatening malignancies
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ruhr University of Bochum

OTHER

Sponsor Role lead

Responsible Party

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Saskia Meves

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Saskia H Meves, MD

Role: PRINCIPAL_INVESTIGATOR

Ruhr University Bochum, Department of Neurology

Other Identifiers

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RUB-Neuro-2013-clopi

Identifier Type: -

Identifier Source: org_study_id

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