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The effect of evolocumab on blood lipids and cardiovascular events in patients with ACS before and after PCI: a multicenter, prospective, randomized controlled trial

The effect of evolocumab on blood lipids and cardiovascular events in patients with ACS before and after PCI: a multicenter, prospective, randomized controlled trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044211
Enrollment
Unknown
Registered
2021-03-12
Start date
2021-03-05
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Acute Coronary Syndrome

Interventions

the group which administer evolocumab before PCI:evolocumab 140mg was applied 1-3 days before PCI, and then use evolocumab 140mg/2w for 6 months.
the group which administer evolocumab after PCI:evolocumab 140mg was administered 2 weeks after PCI, followed by evolocumab 140mg/2w for 6 months.

Sponsors

Tangdu Hospital of Air Force Millitary Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patients who meet all of the following criteria can be included: 1. Aged >= 18 and 30 min; (2) ECG indicates AMI (ST segment elevation >= 0.1 mV or ST segment depression >= 0.1 mV); (3) Myocardial injury markers [myoglobin (Myo), troponin I (cTnI) or creatine kinase isoenzyme (CKMB)] are abnormal. Myo reference value 70%; 4. Sign the written informed consent

Exclusion criteria

Exclusion criteria: Anyone who has one or more of the following cannot be selected for this study: (1) Patients with severe autoimmune diseases or malignant tumors; (2) Patients with severe liver, kidney, brain, and lung dysfunction; (3) Patients with hyperthyroidism or hypothyroidism; (4) Patients with a history of chronic heart failure or cardiomyopathy; (5) Patients who are allergic to statins and PCSK9 inhibitors; (6) Received PCSK9 inhibitor treatment in the past three months; (7) The life expectancy of the patient is <= 12 months; (8) The investigator judges that the patient is not suitable for participating in this study for other reasons; (9) The investigator judged that the patient had poor compliance and could not complete the study as required; (10) Patients who are participating in other clinical trials (except for other topics in this project) but have not reached the time limit of the main research endpoint.

Design outcomes

Primary

MeasureTime frame
the change in lipid parameters;major cardiovascular adverse events;

Secondary

MeasureTime frame
secondary cardiovascular adverse events;Inflammatory factors;PCSK9;

Countries

China

Contacts

Public ContactLi Yan

Tangdu Hospital of Air Force Millitary Medical University

307712565@qq.com+86 13892890227

Outcome results

None listed

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