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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03412435
Other study ID # AMCCV2018-01
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 27, 2018
Est. completion date December 31, 2030

Study information

Verified date December 2023
Source Asan Medical Center
Contact Seung-jung Park, MD
Email sjpark@amc.seoul.kr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study evaluates long-term outcome of patients diagnosed as acute myocardial infarction and treated with medication, coronary artery bypass surgery and percutaneous coronary intervention in Asan medical center, Korea.


Description:

This study will collect 3000 cases retrospectively and 2000 cases prospectively.


Recruitment information / eligibility

Status Recruiting
Enrollment 5000
Est. completion date December 31, 2030
Est. primary completion date December 31, 2025
Accepts healthy volunteers No
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria: - All consecutive acute myocardial infarction patients diagnosed through coronary angiography

Study Design


Locations

Country Name City State
Korea, Republic of Asan Medical Center Seoul

Sponsors (2)

Lead Sponsor Collaborator
Seung-Jung Park CardioVascular Research Foundation, Korea

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary A composite event of all-cause death, non-fatal myocardial infarction and repeat revascularization 1 year
Secondary All cause death 5 year
Secondary Cardiac death 5 year
Secondary Myocardial infarction 5 year
Secondary A composite event of all-cause death and myocardial infarction 5 year
Secondary A composite event of cardiac death and myocardial infarction 5 year
Secondary Repeat revascularization 5 year
Secondary Stent thrombosis according to Academic Research Consortium (ARC) criteria 5 year
Secondary Stroke A stroke or cerebrovascular accident with loss of neurological function caused by an ischemic or hemorrhagic event with residual symptoms at least 24 hours after onset or leading to death. 5 year
Secondary Procedure success Successful percutaneous coronary intervention at the intended target lesion with final instant residual stenosis of less than 30% by quantitative coronary angiography (QCA) and no event of death or Q wave myocardial infarction or urgent revascularization during hospitalization. 7 days
Secondary Surgery success Successful surgery defines as no event of death or Q wave myocardial infarction or urgent revascularization during hospitalization. 7 days
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