Clinical Trial

This Exploratory Medical Device Study Evaluated the Arrhythmia Diagnostic Yield of MEMO Patch V2, a Wearable Patch-type Electrocardiographic Monitor, in Adults With Suspected Arrhythmia Who Presented With Symptoms Such as Palpitations or Dizziness, or Who Had Cryptogenic Ischemic Stroke or Transient

Completed
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Summary
This exploratory medical device study evaluated the arrhythmia diagnostic yield of MEMO Patch V2, a wearable patch-type electrocardiographic monitor, in adults with suspected arrhythmia who presented with symptoms such as palpitations or dizziness, or who had cryptogenic ischemic stroke or transient ischemic attack. The diagnostic yield of MEMO Patch V2 was compared with that of conventional 24-hour ambulatory electrocardiography (Holter monitoring). The study also assessed ECG signal quality, participant compliance, usability and satisfaction, and skin-related adverse events. The findings were intended to provide preliminary data for planning a future large-scale clinical study.
Trial Details
NCT Number NCT07722026
Lead Sponsor HUINNO Co., Ltd
Conditions Suspected Arrhythmia, Palpitations, Dizziness, Cryptogenic Ischemic Stroke, Transient Ischemic Attack
Enrollment 150 participants
Start Date 2021-09-01
Primary Completion 2022-07-05 (estimated)
Study Completion 2022-07-05 (estimated)
Updated on ClinicalTrials.gov 2026-07-23