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Short-term evaluation of modified, low-dose PCSK9 inhibitors combined with statins in the treatment of acute coronary syndrome dyslipidemia in Chinese

Short-term evaluation of modified, low-dose PCSK9 inhibitors combined with statins in the treatment of acute coronary syndrome dyslipidemia in Chinese

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200057772
Enrollment
Unknown
Registered
2022-03-17
Start date
2022-03-13
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

acute coronary syndrome

Interventions

Group 1:receive medium-dose statin daily(atorvastatin 20mg qn or rosuvastatin 10mg qn)
Group 2:receive medium-dose statin daily(atorvastatin 20mg qn or rosuvastatin 10mg qn)+once a month, subcutaneous injection of 1 injection of PCSK9 inhibitor each time
Group 3:receive medium-dose statin daily(atorvastatin 20mg qn or rosuvastatin 10mg qn)+twice a month, subcutaneous injection of 1 injection of PCSK9 inhibitor each time

Sponsors

The First Affiliated Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-85 years, gender unlimited; 2. Diagnosed with acute coronary syndrome; 3. The fasting LDL-C>=1.8mmol/L (70mg/dL); 4. Subjects participated in the study voluntarily and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Uncontrolled hypertension (systolic blood pressure > 180mmHg or diastolic blood pressure > 110mmHg); 2. After treatment, patients with heart failure still have New York grade III-IV or LVEF 3 times the normal value); 6. Lipoprotein or plasma apheresis was performed within one year prior to the start of observation; 7. Patients who are breastfeeding or pregnant; 8. Combined with severe non-cardiovascular disease and life expectancy < 3 years; 9. Patients who are allergic to PCSK9 inhibitors.

Design outcomes

Primary

MeasureTime frame
Total cholesterol;Triglyceride;High density lipoprotein;Low density lipoprotein;Lipoprotein a;

Countries

China

Contacts

Public ContactWang Liansheng
jsyzcxw@163.com+86 13852778870

Outcome results

None listed

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