About this trial
This is a multicenter, open-label, parallel-group, randomized trial to determine if intensive lipid-lowering therapy (goal for LDL-C \<1.0 mmol/L and ≥50% reduction frome baseline) could delay progression of coronary atherosclerotic obstructive leisions compared with guideline recommended lipid-lowering therapy (goal for LDL-C \<1.8 mmol/L and ≥50% reduction frome baseline) among participants between 18-60 years old with non-invasively managed chronic coronary syndrome (at least one lesion with a 50%-70% stenosis).
Eligibility criteria
Qualifiers
None
Disqualifiers
Left main coronary artery disease or severe three-vessel disease;
Ultra-high-risk ASCVD patients: ≥2 severe ASCVD events or 1 severe ASCVD event with ≥2 high-risk factors;
Use of PCSK9 inhibitors or ezetimibe within 8 weeks prior to study enrollment;
The baseline LDL-C was relatively high (LDL-C≥2.6 mmol/L in those taking statins and ≥4.9 mmol/L in those not taking statins).
Trial design
Treatments tested in this trial
- Intensive lipid-lowering strategy
- Standard lipid-lowering strategy
Treatment groups
Sponsors and collaborators
Liu yong
Lead sponsor
Guangdong Provincial People's Hospital
Sponsor institution