Skip to content

The effects of intensive early lipid-lowering and sustained intensive lipid-lowering on atherosclerotic lesion progressin and MACE in patitents with originally diagnosed coronary heart disease- non inferiority, open, randomized controled trial

The effects of intensive early lipid-lowering and sustained intensive lipid-lowering on atherosclerotic lesion progressin and MACE in patitents with originally diagnosed coronary heart disease- non inferiority, open, randomized controled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114667
Enrollment
Unknown
Registered
2025-12-16
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Coronary heart disease

Interventions

Intensive early lipid-lowering:Including cholesterol absorption inhibitors, statins, PCSK9 inhibitors, or lipid-lowering drugs such as inclisiran, a small interfering RNA.
Sustained intensive lipid-lowering (control group):Including cholesterol absorption inhibitors, statins, PCSK9 inhibitors, or lipid-lowering drugs such as inclisiran, a small interfering RNA.

Sponsors

The Seventh Affiliated Hospital Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Originally diagnosed CHD patients with aged between 18-70 years old;

Exclusion criteria

Exclusion criteria: 1. Aged under 18 years or over 75 years; 2.Old myocardial infarction; 3.History of previous coronary artery bypass grafting (CABG) or percutaneous coronary intervention (PCI); 4.History of ischemic or hemorrhagic stroke with residual neurological dysfunction; 5.Symptomatic peripheral vascular disease; 6.More than two severe cardiovascular events occurring consecutively within 2 years; 7.Complicated with middle-advanced stage tumor; 8.Life expectancy = 3 times the upper limit of normal) or renal insufficiency (serum creatinine (Cr) > 1.5 times the upper limit of normal); 10.Known allergy or intolerance to cholesterol absorption inhibitors, statins, proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) and small interfering RNA (siRNA) conjugated to triantennary N-acetylgalactosamine carbohydrates (GalNAc); 11.Baseline New York Heart Association (NYHA) functional class >= III-IV; 12.Pregnancy, lactation period, or ongoing participation in another clinical study.

Design outcomes

Primary

MeasureTime frame
Atherosclerotic lesion progression;Major adverse cardiovascular events;

Secondary

MeasureTime frame
Drug safety;

Countries

China

Contacts

Public ContactJianlei Zheng

The Seventh Affiliated Hospital Sun Yat-sen University

zhengjianlei@sysush.com+86 755 81206787

Outcome results

None listed

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