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临床试验/NCT04955184
NCT04955184已完成不适用

Comparing Cardiac Output Measurements Using a Wearable, Wireless, Non-invasive PPG-Based Device to a Swan Ganz Catheter During Ambulatory Assessment of CHF Patients

Biobeat Technologies Ltd.1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2021年10月10日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
1
主要终点
Comparison of cardiac output obtained by a non-unvasive device to the invasive method

研究概览

简要总结

Invasive pulmonary capillary wedge pressure measurements using a Swan-Ganz catheter (SGC) is considered the gold standard for cardiac output (CO) monitoring. In this prospective study, we will compare CO measurements between a PPG-based wearable monitor and a SGC in ambulatory CHF patients.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 120 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with CHF

排除标准

  • Pregnant women
  • Pediatric patients
  • Inability to sign an informed consent form

结局指标

主要结局

Comparison of cardiac output obtained by a non-unvasive device to the invasive method

时间窗: 2-4 hours per patient

In each participant, a Swan-Ganz catheter will be inserted as part of their routine assessment, and cardiac output measurements will be compared with a non-invasive wearable and wireless PPG-based device.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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