drugset / Trial / NCT06782243

Comparison of High and Moderate Intensity Statins in Achieving the Target LDL-C Level After Acute Coronary Syndrome

NCT06782243

RandomizedParallel-groupOpen-labelTreatment

Summary

This study evaluates the effectiveness of high- and moderate-intensity statins in achieving target low-density lipoprotein cholesterol (LDL-C) levels in patients with acute coronary syndrome (ACS). The study aims to determine whether moderate-intensity statins can provide comparable benefits to high-intensity statins, particularly for patients at higher risk of adverse effects from higher doses. The findings may inform treatment decisions and reduce financial and clinical burdens on patients.

Timeline

Start
2024-12-20
Primary completion
2025-07-30
Completion
2025-08-25

Drugs

EvaluationDrugModalityDoseRoute
Comparator Atorvastatin Small molecule 20 mg Oral
Comparator Atorvastatin Small molecule 40 mg Oral
Comparator Rosuvastatin Small molecule 10 mg Oral
Comparator Rosuvastatin Small molecule 20 mg Oral