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IRIS-Onyx Cohort in the IRIS-DES Registry

S

Seung-Jung Park

Status

Active, not recruiting

Conditions

Coronary Artery Disease
Arterial Occlusive Diseases
Cardiovascular Diseases
Percutaneous Transluminal Angioplasty

Treatments

Device: Onyx Drug Eluting Stent group

Study type

Observational

Funder types

Other

Identifiers

NCT02593994
AMCCV2015-04

Details and patient eligibility

About

The purpose of this study is to evaluate the relative effectiveness and safety of Onyx stent compared to other (drug eluting stents) DES.

Enrollment

4,500 patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 19 and more
  • Intervention with Onyx Drug Eluting Stent
  • Agreed with written informed consent form

Exclusion criteria

  • Intervention with Onyx drug eluting coronary stent and other drug eluting stent at the same time
  • Life expectancy of 1year and under
  • Cardiac shock

Trial design

4,500 participants in 1 patient group

Onyx Drug Eluting Stent
Treatment:
Device: Onyx Drug Eluting Stent group

Trial contacts and locations

31

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Central trial contact

Seung-jung Park, MD, PhD

Data sourced from clinicaltrials.gov

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