跳至主要内容
临床试验/EUCTR2007-002803-42-AT
EUCTR2007-002803-42-AT进行中(未招募)不适用

Inhaled Iloprost for patients with pulmonary arterial hypertension and right heart failure:a pilot feasibility trial

niv.Clinic of Internal Medicine II, Department of Cardiology, Medical University of Vienna, Austria0 个研究点目标入组 8 人开始时间: 2008年2月20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
入组人数
8

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

  • a)PAH classification (according to Pulmonary Hypertension-Executive Summary 2003, Venice
  • b)Echocardiographic and clinical signs of right heart failure, such as dyspnea, tachycardia, edema
  • c)Mean right atrial pressure (mRAP) >15mmHg, cardiac index (CI) <2l/min/m2
  • d)Written informed consent at the time of initial screening in conscious patients. In unconscious patients the treating physician will judge eligibility and the patients have to sign informed consent after regaining consciousness according to the Austrian regulations.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • a)Age younger than 18 years
  • b)Right ventricular failure in the absence of PAH
  • c)Pulmonary venous hypertension due to left-sided atrial, ventricular or valvular heart disease
  • d)Known hypersensitivity to study drug or any ingredient
  • e)Hypertrophic obstructive cardiomyopathy
  • f)Significant aortic stenosis

研究者

发起方
niv.Clinic of Internal Medicine II, Department of Cardiology, Medical University of Vienna, Austria

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