Skip to content

XIENCE Xpedition/Alpine/Sierra in Routine Clinical Practice

Evaluation of Effectiveness and Safety of XIENCE Xpedition/Alpine/Sierra in Routine Clinical Practice; A MULTICENTER, PROSPECTIVE OBSERVATIONAL STUDY

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02042300
Acronym
IRIS XPEDITION
Enrollment
4000
Registered
2014-01-22
Start date
2014-05-31
Completion date
2024-08-30
Last updated
2025-12-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease, Percutaneous Transluminal Coronary Angioplasty

Keywords

XIENCE Xpedition, Routine Clinical Practice, Alpine, Sierra

Brief summary

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

Interventions

DEVICEXIENCE Xpedition/Alpine/Sierra

Sponsors

CardioVascular Research Foundation, Korea
CollaboratorOTHER
Abbott
CollaboratorINDUSTRY
Seung-Jung Park
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Composite event rate1yearDeath, non fatal myocardial infarction, Target Vessel Revascularization

Secondary

MeasureTime frameDescription
Cardiac death5year
Myocardial infarction5year
Composite event of death or myocardial infarction5year
Composite event of cardiac death or myocardial infarction5year
All death5year
Target lesion revascularization5year
Stent thrombosis by an Academic Research Consortium (ARC) criteria5year
Stroke5year
procedural success3daydefined as less than 30% residual stenosis at the completion of procedure without death or Q wave myocardial infarction or urgent revascularization participants will be followed for the duration of hospital stay, an expected average of 3days.
Target Vessel revascularization5year

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026