Dose-Dependent INhibitory Effect of RosuVastatin In Japanese PatienTs with Acute Myocardial InfarcTION on Serum Concentration of Matrix Metalloproteinases

Authors
Category Primary study
Registry of TrialsUMIN Clinical Trials Registry
Year 2015
INTERVENTION: Rosuvastatin 10mg/day (n=60) (Starting dose: 5mg/day) Rosuvastatin 2.5mg/day (n=60) CONDITION: Hypercholesterolemic patients with AMI PRIMARY OUTCOME: The percent change of MMPs at 24 weeks after administration SECONDARY OUTCOME: 1. The change and the changes rate in LDL‐C, HDL‐C, TG, LDL‐C/HDL‐C ratio at 1day, 4weeks, and 24 weeks after administration.; 2. The change and the changes rate of inflammatory markers and cardiac markers at 1day, 4weeks, and 24 weeks after administration. ; 3. The change and the changes rate of inflammatory markers in the aortic root and the coronary sinus at 24 weeks after administration.; 4. The change of the plaque volume and stabilization at 24 weeks after administration.; 5. Correlation between the lipid parameters, inflammatory markers, and other parameters.; 6. Achievement rates of lipid parameters according to guidelines.; 7. Incidence of cerebro‐cardiovascular events.; 8. Incidence and types of adverse events. INCLUSION CRITERIA: Patients meeting the following inclusion criteria will be included in the study: 1) Successful PCI for AMI 2) Hypercholesterolmia (LDL‐C > 100mg/dL) 3) Giving voluntary written consent to participate in the study 4) 20 years old or older
Epistemonikos ID: 54d8990a9ad3a32e76e7c8a5f47fd64a8597f43c
First added on: Aug 23, 2024