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Clinical Trials/NCT01788592
NCT01788592
Recruiting
N/A

Prospective Evaluation of Drug-Eluting Stents in Routine Clinical Practice

Seung-Jung Park1 site in 1 country50,000 target enrollmentJanuary 1, 2003

Overview

Phase
N/A
Intervention
Not specified
Conditions
Coronary Artery Disease
Sponsor
Seung-Jung Park
Enrollment
50000
Locations
1
Primary Endpoint
Major Adverse Cardiac Event
Status
Recruiting
Last Updated
4 months ago

Overview

Brief Summary

The objective of this study is to evaluate effectiveness and safety of drug-eluting stent implantation in the "real world" daily practice.

Registry
clinicaltrials.gov
Start Date
January 1, 2003
End Date
October 1, 2030
Last Updated
4 months ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Seung-Jung Park
Responsible Party
Sponsor Investigator
Principal Investigator

Seung-Jung Park

MD,PhD, Chairman,Heart Institute, Asan Medical Center,University of Ulsan,College of Medicine

Asan Medical Center

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

  • patients with a mixture of several drug eluting stents
  • terminal illness with life expectancy less than 1 year
  • patients with cardiogenic shock

Outcomes

Primary Outcomes

Major Adverse Cardiac Event

Time Frame: 1year

Death from any causes, myocardial infarction or any repeat revascularization

Secondary Outcomes

  • Stent thrombosis by Academic Research Consortium criteria(1year)
  • Myocardial Infarction(1year)
  • Target vessel revascularization(1year)
  • all cause Death(1year)
  • The composite of Death or myocardial infarction(1year)
  • New lesion revascularization(1year)
  • Target lesion revascularization(1year)
  • Any repeat revascularization(1year)

Study Sites (1)

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