跳至主要内容
临床试验/NCT01195805
NCT01195805已完成不适用

The Effect of Amiloride and Spironolactone on Renovascular and Cardiovascular Variables in Patients With Essential Hypertension in a Doubleblinded, Randomized, Placebo-controlled, Crossover Study.

Regional Hospital Holstebro1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2010年8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
发起方
入组人数
25
试验地点
1
主要终点
Bloodpressure

研究概览

简要总结

The investigators wish to study the effect of retaining potassium. The participants have essential hypertension. The test substances are Amiloride, Spironolactone and placebo. The participants will ingest tablets for 28 days before being examined. We will perform a 24 hours urine collection, 24-hours bloodpressure measurement, blood and urine samples and we also examine the patient using a SphygmoCor.

详细描述

Purpose of the study is to examine the effect of amiloride and spironolactone on

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

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
Triple (Participant, Care Provider, Investigator)

入排标准

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

入选标准

  • hypertension,
  • BMI 18,5-30,
  • non-smoker

排除标准

  • Not using contraceptives
  • Other illnesses
  • Drug or alcohol abuse

研究组 & 干预措施

Amiloride

Active Comparator

干预措施: Amiloride (Drug)

Spironolactone

Active Comparator

干预措施: Spironolactone (Drug)

Placebo

Placebo Comparator

1 tablet twice a day for 28 days

干预措施: Placebo (Other)

结局指标

主要结局

Bloodpressure

时间窗: 24-hours and examination

次要结局

未报告次要终点

研究者

发起方
Regional Hospital Holstebro
申办方类型
Other
责任方
Principal Investigator
主要研究者

Erling Bjerregaard Pedersen

professor

Regional Hospital Holstebro

研究点 (1)

Loading locations...

相似试验