Chronic Coronary Syndrome
Conditions
Interventions
Sponsors
Qilu Hospital of Shandong University
Eligibility
Sex/Gender
All
Age
30 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Patients diagnosed with chronic coronary syndrome; 2. Patients aged 30-80 years; 3. Subjects with complete baseline clinical and imaging data required for the study; 4. The volunteers understand and sign the informed consent.
Exclusion criteria
Exclusion criteria: 1. Patients with severe systemic diseases (severe infection, hemorrhagic disease, respiratory failure); 2. Patients with severe hepatic and renal insufficiency (ALT >= 5, ULN (upper limit of normal), Cr > 134) µ 73 m2) or EGFR < 30 ml / min / 1; 3. Patients with malignant tumor and other pathological status with expected survival time less than 1 year; 4. Pregnant or lactating women; 5. Patients who participated in other clinical studies within 12 months before enrollment; 6. Patients with neuropsychiatric diseases.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Composited cardiovascular endpoint; | — |
Secondary
| Measure | Time frame |
|---|---|
| New or recurrent myocardial infarction;First or second revascularization;Stroke;Heart failure;Cardiac death;All-cause death;Recurrent angina;Bleeding event; | — |
Countries
China
Contacts
Public ContactPengfei Zhang
Qilu Hospital of Shandong University
Outcome results
None listed