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临床试验/NCT01388088
NCT01388088已完成4 期

Effect of Amiloride and Spironolactone on Renophysiological and Cardiovascular Variables in Patients With Essential Hypertension in a Doublle-blinded Randomised Placebo-controlled, Cross-over Study.

Erling Bjerregaard Pedersen1 个研究点 分布在 1 个国家目标入组 23 人开始时间: 2010年9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
入组人数
23
试验地点
1
主要终点
Blood pressure

研究概览

简要总结

The investigators wish to investigate the potential effects of potassium. In this study we will examine patients with hypertension and increase their potassium-levels using Amiloride and Spironolactone.

The investigators will examine the changes in the cardiovascular system using a Sphygmocor-scanner.

详细描述

Purpose of the study is to examine the effect of amilorid and spironolacton on

  1. Renal function (GFR, u-AQP2, u-ENaCβ, u-cAMP, u-PGE2, CH20, FENa, FEK),
  2. Pulsewavevelocity, augmentation index and centralt bloodpressure,
  3. Vasoactive hormones (PRC, AngII, Aldo, AVP, ANP, BNP and Endot), and
  4. Ambulatory blood pressure

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
Double (Participant, Investigator)

入排标准

年龄范围
45 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Hypertension
  • Age 45-70
  • BMI: 18,5-30

排除标准

  • Other diseases
  • Drug or alcohol abuse
  • Abnormal findings in the screening procedure

研究组 & 干预措施

Amiloride

Active Comparator

Increases the level of potassium

干预措施: Amiloride (Drug)

Spironolactone

Active Comparator

Increases the level of potassium

干预措施: Spironolactone (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Blood pressure

时间窗: 2 years

24 hours blood pressure measurements

次要结局

  • Pulse wave velocity(2 years)

研究者

发起方
Erling Bjerregaard Pedersen
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Erling Bjerregaard Pedersen

Proffesor

Regional Hospital Holstebro

研究点 (1)

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