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临床试验/NCT01257009
NCT01257009已完成4 期

Atorvastatin Reduces Sympathetic Activity in Patients With Chronic Kidney Disease

UMC Utrecht1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2009年8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
发起方
UMC Utrecht
入组人数
10
试验地点
1
主要终点
Sympathetic activity

研究概览

简要总结

Hypertensive chronic kidney disease (CKD) patients often have sympathetic hyperactivity which appears to contribute to the pathogenesis of hypertension and cardiovascular organ damage. Experimental studies and some clinical studies have shown that statin therapy can reduce central sympathetic activity. Blockade of the renin-angiotensin system (RAS), which is standard treatment for CKD, is known to lower sympathetic activity.

The investigators hypothesize that adding a statin for 6 weeks to RAS blockade would further lower sympathetic activity in hypertensive stage 2-4 CKD patients.

Methods: In ten stable CKD patients who are on chronic treatment with renin-angiotenis blockers, blood pressure and sympathetic activity (quantified by assessment of muscle sympathetic nerve activity, MSNA) will be assessed at baseline and 6 weeks after atorvastatin 20mg/day added.

Ten other CKD patients will serve as time control and will be studied twice with an interval of 6 weeks without any change in medication, to quantify within subject reproducibility.

详细描述

see above

研究设计

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

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • stable chronic kidney disease
  • Hypertension

排除标准

  • renal replacement therapy
  • pregnancy
  • diabetes mellitus

研究组 & 干预措施

1

Other

Arm 1: cessation of any statin therapy for at least 6 weeks, then the first sympathetic activity measurement will be done.Subsequently, atorvastatin 20mg is added for 6 weeks. Then the second sympathetic measurement will be performed.

干预措施: Atorvastatin (Drug)

2

Other

Patients will receive atorvastatin for 6 weeks, then the first sympathetic measurement will be done. Then atorvastatin will be stopped and 6 weeks the second measurement will be done

干预措施: Atorvastatin (Drug)

结局指标

主要结局

Sympathetic activity

时间窗: 4-6 weeks treatment

次要结局

未报告次要终点

研究者

发起方
UMC Utrecht
申办方类型
Other

研究点 (1)

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