IRIS Ultimaster Cohort in the IRIS-DES Registry (IRISUltimaster)

Duk-Woo Park, MD

Status: Completed

Conditions: Coronary Artery Disease

Treatments: Device: Ultimaster stent

Study type: Observational

Funder types: Other

Identifiers

NCT02719106

AMCCV2016-05

Details and patient eligibility

About

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

Enrollment: 1,000 patients

Sex: All

Ages: 19+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age 19 and more
• Intervention with Ultimaster stent
• Agreed with written informed consent form

Exclusion criteria

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

Trial design

1,000 participants in 1 patient group

Ultimaster stent

Treatment:

Device: Ultimaster stent