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
1000 participants
OBSERVATIONAL
2007-05-31
2010-12-31
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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COHORT
PROSPECTIVE
Study Groups
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Acute coronary syndrome
No interventions assigned to this group
Stable Angina
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Age \> 18 years
Exclusion Criteria
* inability to participate in the trial (to give written informed consent)
18 Years
ALL
No
Sponsors
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Martin-Luther-Universität Halle-Wittenberg
OTHER
Responsible Party
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Axel Schlitt
Senior Physician
Locations
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University Clinic of the Martin Luther-University Halle-Wittenberg
Halle, Please Select, Germany
Countries
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Other Identifiers
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CD16PHAMOS
Identifier Type: -
Identifier Source: org_study_id