- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01788592
Prospective Evaluation of Drug-Eluting Stents in Routine Clinical Practice (ASAN PCI Registry)
December 28, 2025 updated by: Seung-Jung Park
Prospective Evaluation of Drug-Eluting Stents in Routine Clinical Practice
The objective of this study is to evaluate effectiveness and safety of drug-eluting stent implantation in the "real world" daily practice.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
50000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Seoul, South Korea
- Recruiting
- Asan Medical Center
-
Principal Investigator:
- Seung-Jung Park, MD,PhD
-
Contact:
- Seung-Jung Park, MD,PhD
- Phone Number: 82-2-3010-4812
- Email: sjpark@amc.seoul.kr
-
Contact:
- Jung-Min Ahn, MD
- Phone Number: 82-2-3010-5904
- Email: drjmahn@gmail.com
-
Sub-Investigator:
- Jung-Min Ahn, MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
consecutive patients amenable to percutaneous coronary intervention with drug eluting stents
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Drug eluting stent
Patients who receiving drug eluting stents
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Major Adverse Cardiac Event
Time Frame: 1year
|
Death from any causes, myocardial infarction or any repeat revascularization
|
1year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Myocardial Infarction
Time Frame: 1year
|
1year
|
|
all cause Death
Time Frame: 1year
|
1year
|
|
The composite of Death or myocardial infarction
Time Frame: 1year
|
1year
|
|
Any repeat revascularization
Time Frame: 1year
|
1year
|
|
Target vessel revascularization
Time Frame: 1year
|
1year
|
|
Target lesion revascularization
Time Frame: 1year
|
1year
|
|
New lesion revascularization
Time Frame: 1year
|
1year
|
|
Stent thrombosis by Academic Research Consortium criteria
Time Frame: 1year
|
1year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Seung-Jung Park, MD, PhD, Asan Medical Center
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2003
Primary Completion (Estimated)
October 1, 2030
Study Completion (Estimated)
October 1, 2030
Study Registration Dates
First Submitted
February 8, 2013
First Submitted That Met QC Criteria
February 8, 2013
First Posted (Estimated)
February 11, 2013
Study Record Updates
Last Update Posted (Estimated)
January 2, 2026
Last Update Submitted That Met QC Criteria
December 28, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AMCCV2013-02
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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