Clinical Trials in China / NCT04184583
Starting soon
Observational
Registry Study on Drug Therapy and Clinical Outcomes in Patients With Acute Coronary Syndrome
NCT04184583 · tracked via the Priya Life Science China tracker
Condition(s) studied
Drug TherapyAcute Coronary Syndrome
Study summary
Registry Study on Drug Therapy and Clinical Outcomes in Patients With Acute Coronary Syndrome
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.
Primary outcome measure(s)
- main adverse cardiovascular and cerebrovascular events (MACCE) — up to 5 years
MACCE will be defined as all-cause death, non-fatal stroke, non-fatal myocardial infarction (MI), and ischemic-driven revascularization.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Beijing Anzhen Hospital | Beijing | Beijing Municipality |
More Beijing Anzhen Hospital trials in China
Other trials for the same condition
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04184583 on ClinicalTrials.gov ↗ ← All trials in China