Skip to content

Evaluation of the First, Second, and New Drug-Eluting Stents in Routine Clinical Practice

Evaluation of Effectiveness and Safety of the First, Second, and New Drug-Eluting Stents in Routine Clinical Practice

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01186133
Acronym
IRIS-DES
Enrollment
50000
Registered
2010-08-23
Start date
2009-01-01
Completion date
2030-12-01
Last updated
2026-06-30

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

coronary disease, drug eluting stent

Brief summary

The objective of this study is to evaluate effectiveness and safety of the new drug-eluting stent (DES), as compared with the first-,second-,third-, and fourth-generation DES, in the "real world" daily practice.

Detailed description

Consecutive patients receiving New DES without a mixture of other DES

Interventions

None listed

Sponsors

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

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* coronary disease amenable to percutaneous coronary intervention (PCI) * no clinical and lesion limitations

Exclusion criteria

* patients with a mixture of several DES * terminal illness with life expectancy less than 1 year * patients with cardiogenic shock

Design outcomes

Primary

MeasureTime frame
Composite of death, nonfatal myocardial infarction (MI), or ischemic-driven Target- Vessel Revascularization (TVR)at 12 months post procedure

Secondary

MeasureTime frame
Death (all-cause and cardiac)at 12 months and annually up to 5 years
Myocardial infarctionat 12 months and annually up to 5 years
Stent thrombosisat 12 months and annually up to 5 years
Target-lesion and target-vessel revascularizationat 12 months and annually up to 5 years
Strokeat 12 months and annually up to 5 years
Procedural successat 1 day

Countries

South Korea

Contacts

CONTACTSeung-Jung Park, MD
sjpark@amc.seoul.kr
CONTACTDuk-Woo Park, MD
dwpark@amc.seoul.kr
STUDY_CHAIRSeung-Jung Park, MD

Asan Medical Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 1, 2026