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临床试验/NCT00932620
NCT00932620已完成4 期

THE EFFECT OF SIMVASTATIN VERSUS COMBINED SIMVASTATIN/EZETIMIBE TREATMENT ON THE CONCENTRATION OF SMALL DENSE LOW-DENSITY LIPOPROTEIN PARTICLES IN PATIENTS WITH PRIMARY HYPERCHOLESTEROLEMIA

University of Ioannina1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2009年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
100
试验地点
1
主要终点
Changes in Small Dense Low-density Lipoprotein Cholesterol (sdLDL-C) Levels

研究概览

简要总结

Both simvastatin 40 mg and simvastatin/ezetimibe 10/10 mg result in low-density lipoprotein cholesterol (LDL-C) reductions of approximately the same magnitude. However, the differential effects of these two treatment options on small dense LDL-C (sdLDL-C) concentration have not been assessed.

The aim of the present study is to compare the effects of simvastatin 40 mg versus simvastatin/ezetimibe 10/10 mg on sdLDL-C concentration. The primary efficacy endpoint will be changes in LDL subfraction profile (i.e. mean LDL particle size, sdLDL-C levels) at 3 months after treatment initiation.

详细描述

Hypercholesterolemia is a major risk factor for atherosclerosis and coronary heart disease (CHD).[1] Epidemiological and clinical studies have demonstrated that aggressive lowering of low-density lipoprotein cholesterol (LDL-C) reduces morbidity and mortality in patients with or without CHD.[1-3] LDL consists of an heterogeneous population of particles with respect to size, density and chemical composition. Several studies have shown that small, dense LDL (sdLDL) particles are more atherogenic than large, buoyant ones[4, 5] and thus associated with increased risk for coronary artery disease[6] or stroke.[7] Statins, the mainstay of lipid lowering therapy, achieve significant reductions in LDL-C levels and are suggested to lower all LDL subfractions, possibly as a result of the statin-induced stimulation of LDL-receptor-mediated catabolism.[8] Moreover, several studies have shown that abnormalities in LDL subfraction profile are amenable to correction with statins.[9] Ezetimibe monotherapy has also been found to significantly reduce concentrations of all LDL subfractions.[10] The combination of ezetimibe with low dose of a statin results in similar LDL-C lowering compared with high dose of the same statin. A recent study demonstrated that ezetimibe/simvastatin combination was more effective than ezetimibe and simvastatin monotherapy in reducing atherogenic lipoprotein subfractions in patients with primary hypercholesterolemia.[11] However, in this study ezetimibe/simvastatin combination was more potent in reducing LDL-C levels compared with either monotherapy.[11] In another study, the addition of ezetimibe in patients already receiving atorvastatin decreased LDL-C values exclusively by reducing the concentrations of large, buoyant LDL subfractions.[12] It is so far unknown whether high-dose of a statin would reduce sdLDL-C level more than low-dose statin plus ezetimibe therapy for the same degree of LDL-C lowering.

Both simvastatin 40 mg and simvastatin/ezetimibe 10/10 mg result in LDL-C reductions of approximately the same magnitude.[13,14] However, the differential effects of these two treatment options on sdLDL-C concentration have not been assessed.

Study design Randomized, open label study.

Aim of the study The aim of the present study is to compare the effects of simvastatin 40 mg versus simvastatin/ezetimibe 10/10 mg on sdLDL-C concentration.

Materials and Methods Study population Consecutive patients with primary hypercholesterolemia (n=100) attending the Outpatient Lipid and Obesity Clinic of the University Hospital of Ioannina, Ioannina, Greece will participate in the present study.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • LDL-C levels above those recommended by the National Cholesterol Education
  • Program Adult Treatment Panel III (NCEP-ATP III) based on each patient risk factors following a 3-month period of lifestyle changes.

排除标准

  • Triglycerides >500 mg/dL, renal disease (serum creatinine levels >1.6 mg/dL), hypothyroidism [thyroid stimulating hormone (TSH) >5 IU/mL] and liver disease (ALT and/or AST levels >3-fold upper limit of normal in 2 consecutive measurements).
  • Patients with hypertension will be included in the study if they are on stable medication for at least 3 months and their blood pressure is adequately controlled (no change in their treatment will be made during the study period).
  • Patients currently taking lipid lowering drugs or having stopped them less than 4 weeks before study entry will be excluded

研究组 & 干预措施

Simvastatin 40 mg

Active Comparator

All subjects will receive dietary instructions according to NCEP-ATP III by a clinical nutritionist. If LDL-C is still above recommended levels after 3 months of appropriate lifestyle changes, patients will be randomly allocated to open-label simvastatin 40 mg (n=50) or simvastatin/ezetimibe 10/10 mg (n=50) daily

干预措施: SIMVASTATIN 40 mg (Drug)

Simvastatin 10 mg plus ezetimibe 10 mg

Active Comparator

All subjects will receive dietary instructions according to NCEP-ATP III by a clinical nutritionist. If LDL-C is still above recommended levels after 3 months of appropriate lifestyle changes, patients will be randomly allocated to open-label simvastatin 40 mg (n=50) or simvastatin/ezetimibe 10/10 mg (n=50) daily

干预措施: SIMVASTATIN/EZETIMIBE 10/10 mg (Drug)

结局指标

主要结局

Changes in Small Dense Low-density Lipoprotein Cholesterol (sdLDL-C) Levels

时间窗: Baseline and 3 months

次要结局

  • Changes in Low-density Lipoprotein Cholesterol (LDL-C)(3 months)

研究者

申办方类型
Other

研究点 (1)

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