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临床试验/JPRN-UMIN000000912
JPRN-UMIN000000912已完成未知

A Study To verify the efficacy of ROsuvastatin 5 mg as an aggressive lipid lowering therapy for hypercholesterolemia (No.2) - ASTRO-2

Graduate School of Medicine, the University of Tokyo0 个研究点目标入组 900 人开始时间: 2007年11月30日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
900

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Patients with severe hypertension (SBP >= 180mmHg or DBP >= 110mmHg) 2) Patients with type I diabetes 3) Patients with familial hypercholesterolemia 4) Patients with fasting serum TG >= 400 mg/dL 5) Patients who have experienced myocardial infarction or a cerebral stroke within 3 months 6) Patients with serious heart failure (NYHA class III to IV) 7) Patients who is scheduled to undergo PTCA/CABG during the study period 8) Patients with active hepatic disease (ALT or AST > 100 IU/L or total bilirubin > 2.5 mg/dL) 9) Patients with renal disorder (Cr >= 2.0 mg/dL or Ccr < 30 mL/min/1.73m2) 10) Patients with CK > 1000 IU/L 11) Patients with hypothyroidism, hereditary muscular diseases (muscular dystrophy, etc.) or familial history of these diseases. Patients with history of drug-related muscular disorder 12) Patients with drug abuse or alcoholic 13) Pregnant women, impregnable women, or those who hope to be pregnant during the study period 14) Patients who use the prohibited concomitant drugs* or who might use such drugs during the study period (* statins, fibrates, cholesterol absorption inhibitors, or probucol) 15) Patients who are ineligible in the opinion of the investigator NB: For values of the tests mentioned above, it is available to use the latest value measured within 6 months of consent agreement.

研究者

发起方
Graduate School of Medicine, the University of Tokyo

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