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Clinical Trial Summary

Heart failure (HF) is a major cardiovascular disease with high readmission and mortality rate. A wearable device that could remotely monitor and detect the worsening HF early before the symptoms appear will help reduce HF readmissions effectively. The purpose of the current study is to examine the efficiency of a novel wearable device based on flexible strain sensor comparing to the clinical 'gold standard,' and then transform it into a clinical application.


Clinical Trial Description

The prospective cohort study aims to examine the efficiency of a novel wearable device based on a flexible strain sensor to improve the outcomes of patients with HF compared to the standard-of-care without wearable device monitoring. The primary and secondary endpoints will be examined in subgroups determined by baseline variables reflecting demography,NYHA functional class,left ventricular ejection fraction,natriuretic peptide,additional co-morbidities,and others. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05642650
Study type Interventional
Source China-Japan Friendship Hospital
Contact Di Sun, Dr.
Phone 010-84206809
Email sundi0929@163.com
Status Not yet recruiting
Phase N/A
Start date February 7, 2023
Completion date April 30, 2025

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