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Investigation of the impact of Evolocumab on the one-year prognosis in patients with acute coronary syndrome following coronary artery bypass grafting

Investigation of the impact of Evolocumab on the one-year prognosis in patients with acute coronary syndrome following coronary artery bypass grafting

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112714
Enrollment
Unknown
Registered
2025-11-18
Start date
2022-12-15
Completion date
Unknown
Last updated
2025-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Atherosclerotic Heart Disease

Interventions

PCSK9 inhibitor combination treatment group (experimental group):Patients in the experimental group were treated with evolocumab, a PSCK9 inhibitor, in addition to their original statin (140 mg subcut
Intensive statin treatment group (control group):Patients in the control group were treated with an intensive statin or a maximum tolerated dose of statin.

Sponsors

Beijing Anzhen Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) age > 18 years old; (2) admission due to acute coronary syndrome; (3) planned to undergo CABG in Beijing Anzhen Hospital; (4) LDL-C >70 mg/dL (1.8mmol/l) after at least 4 weeks of moderate-intensity statin therapy; (5) Patients were voluntarily enrolled in this study and signed informed consent.

Exclusion criteria

Exclusion criteria: (1) allergy to, intolerance to or contraindication to statin or Evolocumab; (2) patients previously treated with Evolocumab or ezetimibe; (3) heart failure (NYHA class III-IV) persisted after continuous therapy; (4) left ventricular ejection fraction 400mg/dL; (6) previous history of hemorrhagic stroke; (7) renal insufficiency (creatinine clearance rate < 30 mL/min); (8) life expectancy less than 1 year; (9) lactating or pregnant patients.

Design outcomes

Primary

MeasureTime frame
Major Adverse Cardiac Events;

Secondary

MeasureTime frame
Non-fatal myocardial infarction;Fatal or non-fatal ischemic stroke;Unstable angina pectoris that requires hospitalization treatment;Coronary death;Coronary artery re-revascularization ;Cardiovascular death;All-cause mortality;

Countries

China

Contacts

Public ContactDongmei Shi

Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University

18910778615@163.com+86 189 1077 8615

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026