Acute Coronary Syndrome
Conditions
Keywords
Acute coronary syndrome, intensive lipid-lowering, statins
Brief summary
In summary, the CHILLAS study will be the first multicenter study performed in a Chinese population using a patient-level analysis to compare the effects and safety of intensive statin therapy with that of moderate statin therapy. Therefore, it will determine whether lower is better, that is, whether LDL cholesterol lowering to a level of approximately 100mg/dl provides a benefit inferior to that of LDL cholesterol lowering to a much lower level; examine the role of inflammatory markers in predicting cardiac events and response to statin therapy; and evaluate the effects of statin therapy on regression of coronary atherosclerosis using IVUS.
Detailed description
The CHILLAS study is planned to evaluate whether intensive treatment with statins for 2 years results in a reduction of cardiovascular events in patients with ACS. A total of 1,600 patients will be randomly assigned to receive intensive statin therapy (atorvastatin, 20 or 40 mg/d, or equivalent dose of other statins) or moderate therapy (atorvastatin, 10 mg/d, or equivalent dose of other statins). Both groups receive dietary counseling. Over a 2-year follow-up period, the primary outcome measure is the time to occurrence of cardiac death, nonfatal acute myocardial infarction, revascularization with either percutaneous coronary intervention or coronary-artery bypass grafting, documented unstable angina or severe heart failure requiring emergency hospitalization, and stroke. The planned duration is between December 2006 and December 2009.
Interventions
DRUGAtorvastatin
Eligible patients are randomly assigned (1:1 ratio) by center to intensive statin therapy (atorvastatin, 20 or 40 mg/d, or equivalent dose of other statins)
Sponsors
Ministry of Science and Technology of the People´s Republic of China
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Clinical diagnosis of acute coronary syndrome * Clinically stable for 24 hours
Exclusion criteria
* Hypersensitive to statins * Receiving therapy with atorvastatin at a dose greater than 20 mg per day before enrollment or lipid-lowering therapy with fibric acid derivatives or niacin that can not be discontinued * Having a coexisting condition that shortened expected survival to less than two years * Having obstructive hepatobiliary disease or other serious hepatic or kidney disease * Having an unexplained elevation in the creatine kinase level that was more than three times the upper limit of normal and that was not related to myocardial infarction * Having undergone surgery or serious trauma within the preceding two months * Having been in the final stage of chronic congestive heart failure * Having a baseline level of LDL cholesterol less than 50mg/dl
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cardiac death, nonfatal AMI, revascularization with either percutaneous coronary intervention or coronary-artery bypass grafting, documented unstable angina or severe heart failure requiring emergency rehospitalization, and stroke | 2 years |
Secondary
| Measure | Time frame |
|---|---|
| The secondary endpoints include total mortality | 2 years |
| LDL cholesterol success rate | 2 years |
| Percentage rate of plaque regression | 2 years |
| In addition, changes in CRP from baseline to specified measurement time points will be calculated | 2 years |
Countries
China
Outcome results
None listed