跳至主要内容
临床试验/CTRI/2009/091/000713
CTRI/2009/091/000713
已完成
未知

Adherent Monitoring of Congestive Heart Failure during Therapy for Excess Fluid (ACUTE) Study

Corventis Inc0 个研究点目标入组 60 人待定

概览

阶段
未知
干预措施
未指定
疾病 / 适应症
Health Condition 1: null- Congestive Heart Failure (CHF)
发起方
Corventis Inc
入组人数
60
状态
已完成
最后更新
4年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
待定
最后更新
4年前
研究类型
Interventional

研究者

发起方
Corventis Inc

入排标准

入选标准

  • Potential patients must meet all of the following criteria:
  • 1\.Is female or male, 18 years of age or older
  • 2\.Has an ejection fraction of 40% reported within 12 months of enrollment
  • 3\.Have acute decompensated heart failure and receiving treatment for fluid overload
  • 4\.Is willing to provide written informed consent and comply with study guidelines

排除标准

  • Patients will be excluded from the study if they meet any of the following criteria
  • 1\.Has an implantable device with an active minute ventilation sensor
  • 2\.Has a known allergy or hypersensitivity to adhesives or hydrogel
  • 3\.Has received the first treatment for this episode of acute heart failure decompensation more than 24 hours ago
  • 4\.Is participating in another clinical study that may confound the results of this study

结局指标

主要结局

未指定

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