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Evolocumab in the Cath Lab for Lipoprotein (a) Lowing in Patients with Acute Myocardial Infarction (EVOLUTION) - A Randomized, Open-label, Blank-controlled, Multicenter Study

Evolocumab in the Cath Lab for Lipoprotein (a) Lowing in Patients with Acute Myocardial Infarction (EVOLUTION) - A Randomized, Open-label, Blank-controlled, Multicenter Study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074191
Enrollment
Unknown
Registered
2023-08-01
Start date
2023-08-01
Completion date
Unknown
Last updated
2023-08-07

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

Conditions

Acute myocardial infarction

Interventions

Trial group:Evolocumab and standard treatment
Control group:Standard treatment

Sponsors

The First Affiliated Hospital of Ningbo University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age =18 years and =80 years old (2) Completion of coronary angiography within 24 h (72 h for NSTEMI) of the onset of typical symptoms, electrocardiograms, or myocardial enzyme profiles. (3) The diagnosis of ASCVD-related myocardial infarction is clear from coronary angiography, and immediate PCI is required. (4) Patients gave informed consent, participated in the study voluntarily and signed an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Unable to complete the follow-up (including but not limited to Killip grade IV or other basic clinical instability as judged by the investigator, patient's inability to co-operate, or combination of other serious diseases, etc.). (2) Contraindication to the use of PCSK9 inhibitors (severe allergies, etc.). (3) Previous application of any type of PCSK9 inhibitor (4) Clearly statin intolerant people (5) Allergic reaction immediately after coronary angiography (6) Recent application (within 3 months) of other biologics, immunosuppressants, immunomodulators, antimetabolite drugs. (7) Dialysis treatment status (8) Combined active malignant tumours, immune system diseases requiring treatment, serious infections and other diseases that may affect the prognosis (9) Women who are planning to become pregnant or are pregnant or breastfeeding. (10) Enrolled in other clinical trials that may affect the purpose or outcome of the study. (11) Other conditions that the investigator considers inappropriate for participation in this trial.

Design outcomes

Primary

MeasureTime frame
Lipid levels;Rate of lipoprotein(a) decline ;

Secondary

MeasureTime frame
NT-proBNP;Inflammatory factors;Cardiovascular events;Adverse Event;Serious Adverse Event;

Countries

China

Contacts

Public ContactXiaomin Chen

The First Affiliated Hospital of Ningbo University

chxmin@hotmail.com+86 138 0588 0193

Outcome results

None listed

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