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Prospective Pecutaneous Coronary Intervention Registry

Prospective Registry for Identifying Long-term Prognosis in Patients Who Underwent Coronary Angiography and Percutaneous Coronary Intervention for Coronary Artery Disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05624905
Acronym
SMC-PCI
Enrollment
15000
Registered
2022-11-22
Start date
2016-03-20
Completion date
2030-12-31
Last updated
2024-08-14

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

Conditions

Coronary Artery Disease, Percutaneous Coronary Intervention

Brief summary

Coronary artery disease is the most important cause of death worldwide. Treatment option for coronary artery disease is medical treatment, percutaneous coronary intervention, or coronary artery bypass surgery. Among them, the field of percutaneous coronary intervention is rapidly developing with regard to the improvement of devices, techniques, or medical treatment, leading to reduce mortality or morbidity. Until now, numerous previous studies related to the risk factors of coronary artery disease and the prognosis of patients have been conducted. However, the field of percutaneous coronary intervention is rapidly evolving, and treatment strategies are constantly being updated. Therefore, the current study sought to identify the long-term prognosis and related risk factors of patients with coronary artery disease who underwent percutaneous coronary intervention.

Interventions

PROCEDUREPercutaneous coronary intervention

Percutaneous Coronary Intervention Procedure

Sponsors

Samsung Medical Center
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

* patients who have undergone or are scheduled to undergo coronary angiography and percutaneous coronary intervention.

Exclusion criteria

* patients who did not consent to the research

Design outcomes

Primary

MeasureTime frameDescription
Rates of Cardiac death or Target-vessel myocardial infarctionup to 10 yearsA composite of cardiac death or target vessel myocardial infarction
Rates of Major adverse cardiac and cerebrovascular eventup to 10 yearsA composite of all-cause death, myocardial infarction, cerebrovascular accident, or repeat revascularization

Secondary

MeasureTime frameDescription
Rates of myocardial infarctionup to 10 yearsAny myocardial infarction
Rates of target-vessel myocardial infarctionup to 10 yearstarget-vessel myocardial infarction
Rates of target lesion revascularizationup to 10 yearstarget lesion revascularization
Rates of all-cause deathup to 10 yearsDeath from any cause
Rates of cerebrovascular accidentup to 10 yearsischemic or hemorrhagic stroke
Rates of stent thrombosisup to 10 yearsdefinite or probable stent thrombosis
Rates of target vessel revascularizationup to 10 yearstarget vessel revascularization
Rates of cardiac deathup to 10 yearsDeath from cardiac cause

Countries

South Korea

Contacts

Primary ContactJoo-Yong Hahn, MD
jyhahn@skku.edu82-2-3410-3419
Backup ContactKi Hong Choi, MD
cardiokh@gmail.com82-2-3410-6653

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026