Status:

COMPLETED

A Clinical Trial to Evaluate the Detection of Atrial Fibrillation for an One Day Versus More Than or Equal to Eight Days Using MEMO Patch PLUS in Individuals Aged ≥ 75 Years, or Those at High Risk of Stroke

Lead Sponsor:

Yonsei University

Conditions:

Atrial Fibrillation/Flutter in Patients With High Risk of Stroke

Eligibility:

All Genders

19+ years

Phase:

NA

Brief Summary

The purpose of this study is to evaluate the benefits in the atrial fibrillation detection rate of the continuous ECG monitoring group for more than 8 days by contrasting with one-day ECG monitoring u...

Eligibility Criteria

Inclusion

  • \[Inclusion criteria\]
  • A participant will be eligible for inclusion in the study if the participant:
  • Has provided documented informed consent for the study.
  • Is adult at least 19 years of age on the day of providing documented informed consent
  • Is the high risk group for stroke, i.e. adult at least 75 years of age or CHA2DS2-VASc score more than 2
  • Is life expectancy more than 6 months
  • Has no Atrial fibrillation or Atrial flutter as a result of 12-lead ECG
  • Has symptoms associated with Atrial fibrillation \*symptoms associated with Atrial fibrillation: palpitation, dizziness, dyspnea, syncope, stroke/transient ischemic accident, systemic embolism etc.
  • \[Exclusion criteria\]
  • The participant must be excluded from the study if the participant:
  • Has had prior history of Atrial fibrillation or Atrial flutter
  • Has received prior or ongoing anticoagulant or antiplatelet therapy
  • Has inserted Pacemaker or Defibrillator that can diagnose Atrial fibrillation or Atrial flutter
  • Has plan of Carotid endarterectomy or inserting Stent\* within 90 days on the day of providing document informed consent \*Stent insertion: means when stent-related interventions have been performed on the carotid arteyr or coronary arteries.

Exclusion

    Key Trial Info

    Start Date :

    May 9 2022

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    July 31 2024

    Estimated Enrollment :

    1000 Patients enrolled

    Trial Details

    Trial ID

    NCT05355948

    Start Date

    May 9 2022

    End Date

    July 31 2024

    Last Update

    September 26 2025

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    Yonsei University Health System, Severance Hospital

    Seoul, South Korea