Acute Coronary Syndrome Clinical Trial
Official title:
Registry Study on Drug Therapy and Clinical Outcomes in Patients With Acute Coronary Syndrome
Registry Study on Drug Therapy and Clinical Outcomes in Patients With Acute Coronary Syndrome
Status | Not yet recruiting |
Enrollment | 10000 |
Est. completion date | December 2026 |
Est. primary completion date | December 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Informed consent has been signed. - Patients diagnosed in our hospital with acute coronary syndrome. - Age =18. - Life expectancy =12 months. Exclusion Criteria: - Severe lack of important information such as history of previous medication, history of previous disease, history of surgery. - Pregnant and lactating women. - Mental disorders, or inability to communicate effectively with researchers, or failure to comply with research protocols. |
Country | Name | City | State |
---|---|---|---|
China | Beijing Anzhen Hospital | Beijing | Beijing |
Lead Sponsor | Collaborator |
---|---|
Beijing Anzhen Hospital |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | main adverse cardiovascular and cerebrovascular events (MACCE) | MACCE will be defined as all-cause death, non-fatal stroke, non-fatal myocardial infarction (MI), and ischemic-driven revascularization. | up to 5 years | |
Secondary | Adverse drug reaction | Adverse drug reaction will be defined as any adverse reactions in the patients. | up to 5 years |
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