跳至主要内容
临床试验/EUCTR2007-004271-19-HU
EUCTR2007-004271-19-HU
进行中(未招募)
不适用

A Phase II/III, Multicenter, Randomized, Double-blind, Placebo-ControlledStudy to Evaluate the Efficacy and Safety of Relaxin in Subjects With Acute Heart Failure. - RELAX-AHF

Corthera, Inc.0 个研究点目标入组 1,160 人2007年11月22日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
未指定
发起方
Corthera, Inc.
入组人数
1160
状态
进行中(未招募)
最后更新
13年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2007年11月22日
结束日期
待定
最后更新
13年前
研究类型
Interventional clinical trial of medicinal product
性别
All

研究者

入排标准

入选标准

  • \- Hospitalized for acute heart failure
  • \- Dyspnea at rest or with minimal exertion
  • \- Pulmonary congestion
  • \- Able to provide informed consent
  • \- Systolic blood pressure \> 125 mmHg
  • \- Impaired renal function defined as an eGFR of 30\-75 mL/min/1\.73m2
  • 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

排除标准

  • \- Use of other IV therapies for acute heart failure
  • \- Fever or sepsis
  • \- Recent major neurologic event
  • \- Recent major surgery
  • \- Recent acute coronary syndrome
  • \- Other recent investigational drug use

结局指标

主要结局

未指定

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