Practice Change With Drug-coated Balloon in Patients With multiVessel Coronary Artery Disease

NCT06104033 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2023-10-27

No results posted yet for this study

Summary

This study is a prospective, multicenter, open-label, observational study to investigate the impact of using drug-coated balloons (DCBs) in the treatment of coronary artery lesions in patients with multivessel coronary artery disease (MVD), as opposed to the default strategy of using only drug-eluting stents (DES). The investigators aim to assess changes in clinical practice towards a hybrid treatment strategy (DES and DCB) and its effects on clinical outcomes.

Conditions

Interventions

DEVICE

drug-coated balloon

For the procedure, the drug-coated balloon (Agent®, Boston Scientific, USA) that can be used for both de-novo coronary lesions and in-stent restenosis lesions is used.

DEVICE

drug-eluting stent

When using drug-eluting stents, the latest 2nd generation drug-eluting stent (Synergy®, Boston Scientific, USA) should be used in accordance with the latest guidelines.

Sponsors & Collaborators

  • Seoul National University Hospital

    collaborator OTHER
  • St Vincent's Hospital

    collaborator OTHER
  • Uijeongbu St. Mary Hospital

    collaborator OTHER
  • Gachon University Gil Medical Center

    collaborator OTHER
  • Gangnam Severance Hospital

    collaborator OTHER
  • Kyunghee University Medical Center

    collaborator OTHER
  • Keimyung University Dongsan Medical Center

    collaborator OTHER
  • Inje University Ilsan Paik Hospital

    collaborator OTHER
  • Daegu Catholic University Medical Center

    collaborator OTHER
  • Sejong General Hospital

    collaborator OTHER
  • Seoul National University Bundang Hospital

    collaborator OTHER
  • Soonchunhyang University Hospital

    collaborator OTHER
  • Yeungnam University Hospital

    collaborator OTHER
  • Wonju Severance Christian Hospital

    collaborator OTHER
  • Ulsan University Hospital

    collaborator OTHER
  • Ewha Womans University Mokdong Hospital

    collaborator OTHER
  • Inje University

    collaborator OTHER
  • Chonnam National University Hospital

    collaborator OTHER
  • Chung-Ang University Gwangmyeong Hospital

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

    collaborator OTHER
  • Ulsan Medical Center

    collaborator OTHER
  • Hanyang University Seoul Hospital

    collaborator OTHER
  • Jeju National University Hospital

    collaborator OTHER
  • KangWon National University Hospital

    collaborator OTHER
  • Uijeongbu Eulji Medical Center, Eulji University

    collaborator UNKNOWN
  • Seoul St. Mary's Hospital

    collaborator OTHER
  • Gyeongsang National University Hospital

    collaborator OTHER
  • Severance Hospital

    collaborator OTHER
  • Chosun University Hospital

    collaborator OTHER
  • Kyungpook National University Hospital

    collaborator OTHER
  • Korea University Anam Hospital

    collaborator OTHER
  • Kyung Hee University Hospital at Gangdong

    collaborator OTHER
  • Ajou University School of Medicine

    collaborator OTHER
  • Bon-Kwon Koo

    lead OTHER

Principal Investigators

  • Bon-Kwon Koo, MD, PhD · +82-2-2072-2062

Eligibility

Min Age
19 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-09-18
Primary Completion
2025-08-31
Completion
2026-10-31

Countries

  • South Korea

Study Locations

More Related Trials

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 NCT06104033 on ClinicalTrials.gov