Adding Antiplatelet During Edoxaban Treatment in Stroke Patients With Non-valvular Atrial Fibrillation (ADD-ON)

NCT04010955 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 1200

Last updated 2025-07-11

No results posted yet for this study

Summary

This study aims to compare the effectiveness and safety regarding treatment with standard anticoagulant only or adding antiplatelet to anticoagulant in patients with non-valvular atrial fibrillation and significant atherosclerosis including extracranial, intracranial, coronary or peripheral artery.

Conditions

  • Acute Ischemic Stroke
  • Atrial Fibrillation
  • Extracranial Atherosclerosis
  • Intracranial Atherosclerosis
  • Coronary Artery Atherosclerosis
  • Peripheral Artery Stenosis
  • Anticoagulant
  • Antiplatelet

Interventions

DRUG

Edoxaban Monotherapy

when the patients will be initially registered in this study, duty physicians will make a decision to give additional antiplatelet therapy in addition to standard edoxaban therapy.

Sponsors & Collaborators

  • Samsung Medical Center

    collaborator OTHER
  • Myongji Hospital

    collaborator OTHER
  • Ewha Womans University

    collaborator OTHER
  • Chonbuk National University

    collaborator OTHER
  • Pusan National University Hospital

    collaborator OTHER
  • Korea University Ansan Hospital

    collaborator OTHER
  • Keimyung University Dongsan Medical Center

    collaborator OTHER
  • Chonnam National University Hospital

    collaborator OTHER
  • Korea University Guro Hospital

    collaborator OTHER
  • Chungnam National University Hospital

    collaborator OTHER
  • Chung-Ang University Hosptial, Chung-Ang University College of Medicine

    collaborator OTHER
  • Kyungpook National University Hospital

    collaborator OTHER
  • Dongtan Sacred Heart Hospital

    collaborator OTHER
  • Eulji University Hospital

    collaborator OTHER
  • Asan Medical Center

    lead OTHER

Principal Investigators

  • Sun U. Kwon, MD, PhD · Asan Medical Center

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-10-08
Primary Completion
2025-06-27
Completion
2026-06-27
FDA Drug
Yes

Countries

  • South Korea

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04010955 on ClinicalTrials.gov