跳至主要内容
临床试验/EUCTR2008-007689-52-EE
EUCTR2008-007689-52-EE
进行中(未招募)
不适用

A Randomized, Double-Blind, Active-Controlled, Multicenter Study of Patients with Cardiovascular Disease and Diabetes Mellitus Not Adequately Controlled with Simvastatin 20 mg or Atorvastatin 10 mg: A Comparison of Switching to a Combination Tablet Ezetimibe/Simvastatin (10mg/20mg) Versus Switching to Rosuvastatin 10mg or Doubling the Statin Dose

Merck & Co. Inc.0 个研究点目标入组 800 人2009年4月16日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
未指定
发起方
Merck & Co. Inc.
入组人数
800
状态
进行中(未招募)
最后更新
13年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2009年4月16日
结束日期
待定
最后更新
13年前
研究类型
Interventional clinical trial of medicinal product
性别
All

研究者

入排标准

入选标准

  • Patients with diabetes mellitus (Type 1 or 2\) with cardiovascular disease, \>\=18 and \<80 years of age with inadequately controlled lipids, either statin/ezetimibe naïve or on an acceptable stable dose, and willing to maintain a cholesterol\-lowering and glucose\-lowering diet for the duration of the study. Baseline LDL\-C must be between \= 70 mg/dL (1\.81 mmol/L) and \= 160 mg/dL (4\.14 mmol/L), TG \= 400 mg/dL (4\.52 mmol/L), ALT/AST \= 2\.0 X ULN, and CK \= 3\.0 X ULN.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range

排除标准

  • Patient is Asian, is hypersensitive/intolerant to any component of the study medication, has CHF NYHA Class III or IV, is an uncontrolled hypertensive or diabetic, or is actively trying to lose weight. Prohibited medications include CYP3A4 inhibitors, lipid\-lowering agents, systemic corticosteroids, anti\-obesity medications, warfarin, or medications that could increase the risk of myopathy.

结局指标

主要结局

未指定

相似试验

进行中(未招募)
不适用
The study is to evaluate the effectiveness and safety of switching to coadministration ezetimibe and atorvastatin compared with doubling the dose of atorvastatin or switching to rosuvastatin in patients with primary hypercholesterolemia and high cardiovascular risk who are not adequately controlled with atorvastatin 10 mg. Ezetimibe, atorvastatin and rosuvastatin are each available by prescription to treat high blood cholesterol levels.
EUCTR2009-015247-16-DEMerck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.1,508
进行中(未招募)
不适用
A Randomized, Double-Blind, Active-Controlled, Multicenter Study of Patients with Primary Hypercholesterolemia and High Cardiovascular Risk Who Are Not Adequately Controlled with Atorvastatin 10 mg: A Comparison of the Efficacy and Safety of Switching to Coadministration Ezetimibe and Atorvastatin Versus Doubling the Dose of Atorvastatin or Switching to Rosuvastatin - SWITCH
EUCTR2009-015247-16-SKMerck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.1,508
进行中(未招募)
1 期
A Randomized, Double-Blind, Active-Controlled, Multicenter Study to Assess the LDL-C Lowering of Switching to a Combination tablet Ezetimibe/Simvastatin (10mg/20mg) compared to Rosuvastatin 10mg in patients with primary hypercholesterolemia and high cardiovascular risk and not adequately controlled with a prior statin treatment. (IN-CROSS). - IN-CROSS
EUCTR2006-005513-35-LTMerck&co., Inc.1,200
进行中(未招募)
1 期
A Randomized, Double-Blind, Active-Controlled, Multicenter Study to Assess the LDL-C Lowering of Switching to a Combination tablet Ezetimibe/Simvastatin (10mg/20mg) compared to Rosuvastatin 10mg in patients with primary hypercholesterolemia and high cardiovascular risk and not adequately controlled with a prior statin treatment. (IN-CROSS).
EUCTR2006-005513-35-NL300
进行中(未招募)
1 期
A Randomized, Double-Blind, Active-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of Canagliflozin Versus Sitagliptin in the Treatment of Subjects With Type 2 Diabetes Mellitus With Inadequate Glycemic Control on Metformin and Sulphonylurea Therapy - CANTATA-D2
EUCTR2010-020053-14-BEJanssen-Cilag International NV720