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 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
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
研究者
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