EPICOR-RUS is a multi-centre, observational, prospective, longitudinal cohort study which will include patients, in a real-life setting, who are hospitalized for acute coronary syndrome (ACS) within 24 hours of symptom onset and who have a final diagnosis of Unstable Angina (UA), ST-Elevation Myocardial Infarction (STEMI) or Non-ST-Elevation Myocardial Infarction (NSTEMI). Patients will undergo clinical assessments and receive the standard medical care as determined by the treating cardiologist. Patients will not receive experimental intervention or experimental treatment as a consequence of their participation in the EPICOR-RUS observational study.
Study Type
OBSERVATIONAL
Enrollment
600
Research Site
Barnaul, Russia
Research Site
Cheboksary, Russia
Research Site
Kazan', Russia
Research Site
Kemerovo, Russia
Research Site
Kirov, Russia
Research Site
Krasnodar, Russia
Research Site
Krasnoyarsk, Russia
Research Site
Moscow, Russia
Research Site
Murmansk, Russia
Research Site
N.Novgorod, Russia
...and 9 more locations
Short- and long-term medication and treatment prescribed by physicians in real-life setting
Time frame: up to 2 years
clinical outcome (Cardiovascular events)
Time frame: up to 2 years
quality of life (EQ-5D questionnaire)
Time frame: up to 2 years
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