The primary objective of this study is to compare the effect of rosuvastatin 10mg with atorvastatin 10mg in the percentage reduction of LDL-C in Subjects with metabolic syndrome after 6 weeks of treatment.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
370
Research Site
Daegu, South Korea
Research Site
Iksan, South Korea
Research Site
Jeonju, South Korea
Research Site
Jinju, South Korea
The primary objective of this study is to compare the effect of rosuvastatin 10mg with atorvastatin 10mg in the percentage reduction of LDL-C in Subjects with metabolic syndrome after 6 weeks of treatment.
The secondary objectives of this study are to compare the effects of rosuvastatin 10mg with atorvastatin 10mg in subjects with metabolic syndrome, after 6weeks of treatment, on:
Bringing subjects to their established NCEP ATP III target goals for LDL-C
Bringing subjects to their non-HDL target goal(based on NCEP-ATP III criteria)
Modifying other lipids and lipid ratios
Modifying inflammatory markers
Glucose and insulin resistance
Safety
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Research Site
Kwangju, South Korea
Research Site
Pusan, South Korea
Research Site
Ulsan, South Korea