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Effects of evolocumab on periprocedural myocardial injury in patients with acute coronary syndrome undergoing elective percutaneous coronary intervention

Effects of evolocumab on periprocedural myocardial injury in patients with acute coronary syndrome undergoing elective percutaneous coronary intervention

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104994
Enrollment
Unknown
Registered
2025-06-26
Start date
2021-01-10
Completion date
Unknown
Last updated
2025-06-30

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

Conditions

coronary heart disease

Interventions

experimental group:The patients receive?evolocumab?(140 mg before PCI,once every 2 weeks)
control group:no intervention

Sponsors

The second hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.age between 18-80; 2.sign the Informed consent; 3.Diagnosis of ACS is planned for elective PCI, including unstable angina pectoris (UA), acute non-ST-elevation myocardial infarction (NSTEMI), acute ST-elevation myocardial infarction (STEMI); 4.Patients who took moderate-intensity statins (atorvastatin calcium tablets 20mg-40mg 1/night, or other statins of equivalent strength) for at least 4 weeks before enrollment still had an LDL >= 1.8mmol/L.

Exclusion criteria

Exclusion criteria: 1.Patients with acute myocardial infarction requiring emergency PCI; 2. Patients whose angiography results indicate PCI is either unnecessary or unfeasible; 3.The clinical condition is unstable,such as hemodynamic disorder or malignant arrhythmia, and the life expectancy is less than 3 months; 4.Heart function grade III-IV or EF<30%; 5. Severe renal dysfunction (eGFR<30ml/min); 6. Severe liver function injury, liver enzymes (ALT, AST) increased by more than 3 times; 7.Can not tolerate any dose of statin therapy, such as severe myolysis, liver function damage; 8. Patients with PCSK-9 inhibitor before inclusion; 9. Allergies to PCSK-9 inhibitors, statins and contrast agents; 10. Malignant tumor; 11. Severe ischemic or hemorrhagic brain stroke within 3 months

Design outcomes

Primary

MeasureTime frame
rate of periprocedural myocardial injury and myocardial infarction ;

Secondary

MeasureTime frame
change of blood lipids before and one month after surgery;moniter Adverse Drug Reactions, including CK,AST,ALT,CCr before surgery and at 1 month postoperatively.;rate of MACE;

Countries

China

Contacts

Public ContactXie Yanan

The second hospital of Hebei Medical University

383957760@qq.com+86 158 3115 0835

Outcome results

None listed

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