Prevention of Cardiovascular Events by Antiplatelet Agents After Acute Coronary Syndrome
NCT ID: NCT01952392
Last Updated: 2017-02-24
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
4992 participants
OBSERVATIONAL
2013-10-31
2016-03-31
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
Study Groups
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Control group
Patients aged 18 years or more with an acute coronary syndrome, agreed to participate and able to answer an interview in French and/or providing the details of an alternative replier (proxy) if necessary
No interventions assigned to this group
Case group
Patients aged 18 years or more with a history of acute coronary syndrome (i.e. a recurrent MI after myocardial history or unstable angina), agreed to participate and able to answer an interview in French and/or providing the details of an alternative replier (proxy) if necessary
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
18 Years
130 Years
ALL
No
Sponsors
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AstraZeneca
INDUSTRY
Responsible Party
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Locations
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Research Site
Paris, , France
Countries
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Related Links
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Other Identifiers
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NIS-CFR-BRI-2012/1
Identifier Type: -
Identifier Source: org_study_id
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