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临床试验/NCT01126684
NCT01126684已完成不适用

EFFECTS OF ATORVASTATIN ON BLOOD PRESSURE AND URINARY ALBUMIN EXCRETION IN PATIENTS WITH ESSENTIAL HYPERTENSION

Aristotle University Of Thessaloniki1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2008年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
1
主要终点
Ambulatory blood pressure

研究概览

简要总结

To evaluate the possible effects of atorvastatin on ambulatory blood pressure, urinary albumin excretion, insulin resistance and arterial stiffness in hypertensive patients, beyond those on lipid profile. Glycemic parameters, "novel" cardiovascular risk factors and safety parameters will be also evaluated.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • LDL-C>130 or >160 mg/dL (depending on the total risk according to the most recent recommendations25).
  • no previous hypolipidemic medication
  • ability to provide Informed Consent.

排除标准

  • pregnancy or lactation
  • myocardial infarction or unstable angina within the past 6 months
  • heart failure NYHA class III-IV
  • renal disease (SCr>3 mg/dL or proteinuria>3g/d)
  • liver disease
  • history of malignancy
  • history of drug or alcohol abuse
  • treatment with corticosteroids
  • any other condition with poor prognosis
  • inability to provide Informed Consent.

研究组 & 干预措施

Atorvastatin

Active Comparator

干预措施: Atorvastatin (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Ambulatory blood pressure

时间窗: Six months

次要结局

  • Urinary Albumin Excretion(Six months)
  • Insulin Sensitivity(Six months)
  • Arterial Stiffness(Six months)
  • Urinary levels of nephrin(Six months)
  • Urinary levels of podocalyxin(Six months)
  • Urinary levels of Endothelin-1(Six months)
  • Urinary levels of Asymmetric Dimethylarginine(Six months)
  • Urinary levels of indices of oxidative stress(Six months)

研究者

申办方类型
Other

研究点 (1)

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