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
500 participants
OBSERVATIONAL
2010-04-30
2017-04-30
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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COHORT
PROSPECTIVE
Study Groups
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CAD patients
Representative sample of coronary artery disease patients receiving aspirin therapy for secondary prevention
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients with documented coronary artery disease
* Current treatment with any dose of aspirin daily for a minimum of 3 months
* Able to provide written informed consent based on competent mental status
Exclusion Criteria
* Platelet count \<125,000/mm
* Known haematological disorders
* Active malignancy on current chemotherapy or a recent diagnosis of cancer
18 Years
ALL
No
Sponsors
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Royal College of Surgeons, Ireland
OTHER
Responsible Party
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Prof Dermot Kenny
Prof. Dermot Kenny
Principal Investigators
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Prof. Dermot Kenny, MB, BCh, BAO, MD
Role: PRINCIPAL_INVESTIGATOR
Royal College of Surgeons, Ireland
Locations
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Beaumont Hospital
Dublin, Dublin, Ireland
Countries
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Central Contacts
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Other Identifiers
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INFACTs2010-001
Identifier Type: -
Identifier Source: org_study_id