跳至主要内容
临床试验/EUCTR2011-002587-24-IT
EUCTR2011-002587-24-IT进行中(未招募)不适用

Effects of Aliskiren on microcirculation dysfunction in patients affected by hypertension

FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR0 个研究点开始时间: 2012年1月10日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Age =40 and =75 yr.
  • Body mass index (BMI) =32 kg/m2;
  • Diastolic BP (DBP) <110 mmHg and systolic BP (SBP) <180 mmHg in patients previously treated;
  • On therapy with amlodipine with or without a thiazide diuretic;
  • Left ventricular mass index (LVMI) =115 g/m2 (men) or =100 g/m2 (women) quantified by two dimensional echocardiography;
  • Left ventricular ejection fraction =55% at two-dimensional echocardiography;
  • Valid informed consent obtained from participants.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 24
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 18

排除标准

  • History of secondary HT;
  • Anamnestic coronary heart disease;
  • Renal failure (creatinine >1.69 mg/dl or creatinine clearance <30 ml/min);
  • Hypokalemia (<3.4 mEq/l) or hyperkalemia (>5 mEq/l);
  • Insulin-dependent diabetes;
  • Significant valvular disease or left ventricular systolic dysfunction at echocardiography;
  • Treatment with Aliskiren, ACE inhibitors or angiotensin receptor blockers in the month preceding the first selection visit;
  • Patients with stress-induced regional perfusion defects at PET will be referred for coronary angiography and excluded from the study if they have coronary artery disease;
  • Pregnancy and breastfeeding;
  • ACEI angioedema, hereditary and/or idiopathic angioedema;
  • Severe hepatic dysfunction

研究者

发起方
FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR

相似试验

Effect of Aliskiren drug in patients with high blood... | 临床试验