About this trial

This study aims to analyze the efficacy and safety of wearable electrocardiogram (ECG) monitoring by simultaneously attaching a single-channel patch-type wearable ECG monitoring device (HiCardi+ by Mezoo Co., Ltd.) and a telemetry device (IntelliVue MX40 by Philips) used in actual wards to patients prescribed with ECG monitoring

Eligibility criteria

Qualifiers

Adults aged 19 years or older

Patients admitted to Chonnam National University Hospital who require ECG monitoring

Individuals who have expressed their intention to participate in this study or have obtained written consent from a proxy

Disqualifiers

Individuals who are unable to provide consent themselves or through a legally designated representative

Individuals deemed unsuitable for participation in the clinical trial based on the researcher's judgment

Trial design

Treatments tested in this trial

  • ECG monitoring by telemetry device and patch-type ECG monitor at the same time

Treatment groups

100 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators

Mezoo Co., Ltd.

Lead sponsor