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Multicenter real-world observational study of lipid-lowering efficacy assessment of different lipid-lowering strategies in high-risk populations above ASCVD

Multicenter real-world observational study of lipid-lowering efficacy assessment of different lipid-lowering strategies in high-risk populations above ASCVD

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500106915
Enrollment
Unknown
Registered
2025-07-31
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Atherosclerotic Cardiovascular Disease

Interventions

Group of Inclisiran:NA
Traditional treatment group:NA

Sponsors

Shengjing Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients with baseline age >= 18 years, regardless of gender, diagnosed with high risk of ASCVD (refer to 2023 Chinese Blood Lipid Guidelines ); 2. Received moderate doses of statins when participating in the study; 3. Those who received Inclisiran were included in the combination group of Inclisiran, and those who received other lipid-lowering drugs were included in the traditional treatment group.

Exclusion criteria

Exclusion criteria: The combination group of Inxilam needs to exclude those who have received Inclisiran treatment within 2 years before participating in the study or PCSK9 monoclonal antibody within 3 months before participating in the study; Participating in other cardiovascular trials at time of inclusion ; Have severe liver disease (Child-Pugh class C); Severe anemia (hemoglobin <7 g / dl); Autoimmune diseases (systemic lupus erythematosus, etc.); Pregnancy status; Critically ill patients with life expectancy < 15 months.

Design outcomes

Primary

MeasureTime frame
Reduction in LDL-C levels;Rate of achieving LDL-C targets;

Secondary

MeasureTime frame
Change in LDL-C variability;Changes in other lipid parameters;Proportion of patients with lipid-lowering medication PDC >= 80 %;Mean days of coverage;

Countries

China

Contacts

Public ContactZhang Daqing

Shengjing Hospital of China Medical University

zhangdaqing@vip.163.com+86 189 4025 5581

Outcome results

None listed

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