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Clinical Trials in South Korea / NCT01186133
Recruiting Observational

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

NCT01186133 · tracked via the Priya Life Science South Korea tracker
Sponsor
Seung-Jung Park
Phase
Observational
Started
2009-01
Last updated
2026-06-30

Condition(s) studied

Coronary Artery DiseasePercutaneous Transluminal Coronary Angioplasty

Study 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.

Eligibility

Sex
ALL
Min age
19 Years
Max age
—
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

Primary outcome measure(s)

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

Trial sites (1)

FacilityCityRegionStatus
Korean centres Multiple Locations South Korea Recruiting

More Seung-Jung Park trials in South Korea

Study of the Natural History of FFR Guided Percutaneous Coronary Intervention Recruiting
Evaluation of Effectiveness and Safety of Rotational Atherectomy in Routine Clinical Practice Recruiting
Observational Study for Left Main Disease Treatment Recruiting
Asan Multivessel Registry Recruiting
IRIS-Onyx Cohort in the IRIS-DES Registry Active, not recruiting

Other trials for the same condition

Clinical Impact of Orsiro™ Stent in Patient With Chronic Kidney Disease Active, not recruiting
The COMPLETE Treatment of Bifurcation With Two-stent Techniques: Randomized Comparison of Crush Versus Culotte Technique Recruiting
CREATE Trial, Prospective, Observational Study Active, not recruiting
Study of the Natural History of FFR Guided Percutaneous Coronary Intervention Recruiting
Safety and Efficacy of Paclitaxel Coated PTCA Balloon Catheter With a Shellac Plus Vitamin E Excipient (GENOSS® DCB) in Patients With Coronary In-stent Restenosis (ISR): A Prospective, Multi-center, Observational Study Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT01186133 on ClinicalTrials.gov ↗ ← All trials in South Korea