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An Open-label Study of EZYPRO® in Atrial Fibrillation Detection on ESUS Patients

Atrial Fibrillation Clinical Trial

Official title:
An Open-label Study to Evaluate the Effectiveness and Safety of EZYPRO® in Atrial Fibrillation Detection in Nearly Embolic Stroke of Undetermined Source (ESUS) Patient

Clinical Trial Summary

The aim of the study is to evaluate the effectiveness and safety of the 14-day continuous ECG patch monitor (EZYPRO®) compared with a 24-hour Holter monitor in the detection of atrial fibrillation (AF) among ESUS patients.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05089435
Study type Interventional
Source Sigknow Biomedical Co., Ltd.
Contact Nancy Lu
Phone +886227612577
Email nancy.lu@sigknow.com.tw
Status Recruiting
Phase Phase 4
Start date March 28, 2022
Completion date December 2023
View Details
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