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临床试验/NCT00551447
NCT00551447已完成3 期

A Comparison of Treatment With Ezetimibe (SCH 58235) and Simvastatin Coadministration Versus Simvastatin in Attaining the National Cholesterol Education Program (NCEP) Adult Treatment Panel (ATP) III Coronary Heart Disease (CHD) or CHD Risk Equivalent Strata Low-Density Lipoprotein Cholesterol (LDL-c)

Organon and Co0 个研究点目标入组 616 人开始时间: 2002年1月最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
616
主要终点
LDL-C measurement (target goal = <100 mg/dL)

研究概览

简要总结

This purpose of this study is to determine if the administration of ezetimibe and simvastatin together is more effective than simvastatin alone in lowering LDL-C levels to a goal of <100 mg/dL in patients at risk for Heart Disease.

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
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Men and women aged 18 to 80 at risk for Heart Disease who have LDL-C levels greater than or equal to 130 mg/dL and triglyceride level less than or equal to 350 mg/dL
  • Patients must be able to maintain the National Cholesterol Education Program diet throughout the course of the study

排除标准

  • Patients are excluded from the study if their weight is less than 50% of ideal body weight, if they are pregnant or lactating, have congestive heart failure, uncontrolled heart rhythm problems or a recent heart attack, coronary artery bypass surgery, or angioplasty. Additionally, patients with poorly controlled Type 1 or 2 diabetes mellitus, kidney disease, uncontrolled endocrine or metabolic disease, are known HIV positive, and uncontrolled high blood pressure

结局指标

主要结局

LDL-C measurement (target goal = <100 mg/dL)

时间窗: 27 Weeks

次要结局

  • Well tolerated in patients(27 Weeks)

研究者

申办方类型
Industry
责任方
Sponsor

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