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XIENCE Xpedition/Alpine/Sierra in Routine Clinical Practice (IRIS XPEDITION)

S

Seung-Jung Park

Status

Active, not recruiting

Conditions

Coronary Artery Disease
Percutaneous Transluminal Coronary Angioplasty

Treatments

Device: XIENCE Xpedition/Alpine/Sierra

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT02042300
AMCCV2013-11

Details and patient eligibility

About

The purpose of this study is to evaluate effectiveness and safety of XIENCE Xpedition/Alpine/Sierra in Routine Clinical Practice

Enrollment

4,000 patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 19 and more
  • Intervention with XIENCE Xpedition or Alpine or Sierra everolimus eluting coronary stent
  • Agreed with written informed consent form

Exclusion criteria

  • Intervention with XIENCE Xpedition or Alpine or Sierra everolimus eluting coronary stent and other drug eluting stent at the same time
  • Life expectancy of 1year and under
  • Cardiac shock

Trial design

4,000 participants in 1 patient group

IRIS-Xpedition/Alpine/Sierra Cohort
Description:
XIENCE Xpedition/Alpine/Sierra
Treatment:
Device: XIENCE Xpedition/Alpine/Sierra

Trial contacts and locations

26

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Data sourced from clinicaltrials.gov

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