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The effect of PCSK9 inhibitor on platelet function and coagulation function in ACS patients undergoing PCI

The effect of PCSK9 inhibitor on platelet function and coagulation function in ACS patients undergoing PCI

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053229
Enrollment
Unknown
Registered
2021-11-16
Start date
2021-11-01
Completion date
Unknown
Last updated
2022-09-20

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

Conditions

Unstable angina and non-ST-segment elevation myocardial infarction

Interventions

Group 1:Moderate-high intensity statin ± ezetimibe) + ilovolumab 140mg
Group 2:Moderate-to-high-intensity statin dose ± ezetimibe

Sponsors

The Second Hospital of Tianjin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with coronary atherosclerotic heart disease who were admitted to hospital for the first time due to NSTE-ACS and received coronary angiography and PCI; 2. No perioperative complications within 48 hours after PCI; no or discontinuation of other antithrombotic therapy for at least 24 hours; 3. Aged >= 18 years; 4. HyperLDL-C: patients who have received statin ± ezetimibe (>=4 weeks) treatment, LDL-C> 2.2mmol/L; patients who have not received statin ± ezetimibe treatment, LDL-C > 4mmol/L; 5. Agree to join this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Allergy or intolerance to PCSK9 inhibitors, and have used any kind of PCSK9 inhibitor; 2. Platelets 450 x 10^9/L, or other serious blood system diseases; 3. Patients with autoimmune diseases; 4. Patients who are undergoing or need long-term anticoagulation therapy; 5. Patients with liver and renal insufficiency (creatinine clearance rate <30ml/min, ALT/AST exceeding 3 times the upper limit of normal, or history of liver cirrhosis); 6. Combined with malignant tumor or serious infection; 7. Pregnancy.

Design outcomes

Primary

MeasureTime frame
Platelet aggregation rate;Blood lipids;

Secondary

MeasureTime frame
High-sensitivity C-reactive protein;Circulating platelet particles;Blood routine;Soluble P-selectin;

Countries

China

Contacts

Public ContactChe Jingjin

The Second Hospital of Tianjin Medical University

jingjinche@163.com+86 18630918358

Outcome results

None listed

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