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临床试验/EUCTR2009-011558-16-DE
EUCTR2009-011558-16-DE进行中(未招募)不适用

Evaluation of the effects of 4 oral dosages of S 44121 versus placebo on cardiac function and NT-proBNP in patients with chronic heart failure and left ventricular dysfunction. A 12-week, randomized, double-blind, parallel-group, placebo controlled, international multicentre study.

Institut de Recherches Internationales Servier0 个研究点目标入组 150 人开始时间: 2010年1月14日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
150

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

  • - Male or female patients superior or equal to 18 years and less or equal to 75 years.
  • - Symptomatic chronic heart failure for at least 6 months before selection.
  • - NYHA functional class II or III.
  • - Ischemic disease or idiopathic dilated cardiomyopathy as main cause for CHF.
  • - Left ventricular systolic dysfunction as evidenced by a LVEF less or equal to 35 % as measured within 6 months before selection.
  • - Beta-blocker treatment for at least 3 months before selection.
  • - ACE inhibitor and/or an ARB treatment for at least 3 months before selection.
  • - NT-proBNP plasma concentration superior or equal to 400 pg/mL or BNP plasma concentration superior or equal to 100 pg/mL.
  • 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

  • - Unstable condition within the previous 4 weeks before selection.
  • - Recent (less than 3 months before selection) myocardial infarction, unstable angina or coronary revascularisation.
  • - History of stroke or cerebral transient ischemic attack within the previous 3 months before selection.
  • - Severe aortic or mitral stenosis, severe aortic regurgitation, or severe mitral regurgitation.
  • - Congenital heart disease.
  • - Hypertrophic obstructive cardiomyopathy.
  • - Pericardial disease.
  • - Atrio-ventricular block of second or third degree.
  • - Corrected QT interval duration (Bazett’s formula) > 450 ms.
  • - Family history of long QT syndrome or congenital long QT syndrome.
  • - Serum creatinine > 200 micromoles/L (> 2.26 mg/dL).
  • - ALAT or ASAT > 3 times the upper limit of normal values.
  • - Serum total calcium < 2.1 mmol/L or > 2.6 mmol/L.
  • - Blood hemoglobin lower than 110 g/L (in males) or lower than 100 g/L (in females).

研究者

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