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临床试验/NCT00130884
NCT00130884已完成2 期

Effects of Peroral Levosimendan in the Prevention of Further Hospitalisations in Patients With Chronic Heart Failure. A Randomised, Phase II, Double-Blind, Placebo-Controlled, Multi-Centre, Parallel-Group Study

Orion Corporation, Orion Pharma1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2005年3月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
300
试验地点
1
主要终点
Composite endpoint measuring symptoms, morbidity, mortality

研究概览

简要总结

The study will investigate the efficacy of oral levosimendan in patients with chronic New York Heart Association (NYHA) IIIb-IV heart failure (HF) using a composite end-point evaluating patient symptoms, morbidity and mortality. The patients are on treatment for at least 6 months.

详细描述

The patients are randomised to 3 groups; higher or lower levosimendan dose group or placebo.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Diagnosed chronic heart failure
  • •Severe symptoms (NYHA IIIb-IV)
  • •Optimal on-going oral treatment for HF
  • •Left ventricular ejection fraction less than or equal to 30%

排除标准

  • •Severe obstruction of ventricular outflow tracts
  • •Acute myocardial infarction within 30 days before screening
  • •Cardiac surgery or coronary angioplasty within 30 days before screening

结局指标

主要结局

Composite endpoint measuring symptoms, morbidity, mortality

次要结局

未报告次要终点

研究者

申办方类型
Industry

研究点 (1)

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