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临床试验/NL-OMON38730
NL-OMON38730招募中不适用

Primary hyperaldosteronism and endothelial ischemia-reperfusion injury - Primary hyperaldosteronism and ischemia-reperfusion injury

niversitair Medisch Centrum Sint Radboud0 个研究点目标入组 40 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • For patients with primary hyperaldosteronism:
  • -Age 18-75 years
  • -Confirmed primary hyperaldosteronism (aldosterone >0.28 nmol/L after salt loading)
  • -Serum potassium >= 3.5 mmol/L (with or without potassium supplementation)
  • -Written informed consent;For control patients with primary (essential) hypertension:
  • - Age 18-75 years
  • - Primary hypertension
  • - Baseline aldosterone <0.30 nmol/l and ARR<0.09.
  • - Serum potassium >= 3.5 mmol/L
  • - Written informed consent

排除标准

  • -History of atherosclerotic disease (myocardial infarction (MI), stroke, or peripheral vascular disease)
  • -Not possible to change the antihypertensive medication into only diltiazem with or without hydralazine, or to temporarily stop statins according to the treating physician
  • -Severe renal dysfunction (MDRD < 30 ml/min)
  • -Second/third degree AV-block on electrocardiography
  • -Cardiac failure
  • -Diabetes mellitus
  • -Use of acetylsalicylic acid, NSAID*s, theophylline, and dipyridamole

研究者

发起方
niversitair Medisch Centrum Sint Radboud

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