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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02791412
Other study ID # AMCCV2016-08
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 13, 2017
Est. completion date May 30, 2018

Study information

Verified date June 2018
Source Asan Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to evaluate long-term outcome of treatment(percutaneous coronary intervention or coronary-artery bypass graft) in unprotected left main coronary artery stenosis in Korea.


Recruitment information / eligibility

Status Completed
Enrollment 2240
Est. completion date May 30, 2018
Est. primary completion date May 30, 2018
Accepts healthy volunteers No
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria:

- Unprotected left main disease

Exclusion Criteria :

- No exclusion criteria

Study Design


Intervention

Procedure:
percutaneous coronary intervention or coronary-artery bypass graft


Locations

Country Name City State
Korea, Republic of Chungnam National University Hospital Dae-jeon
Korea, Republic of Kyungpook National University Hospital Daegu
Korea, Republic of Chonnam National University Hospital Gwangju
Korea, Republic of Gachon University Gil Hospital Incheon
Korea, Republic of Asan Medical Center Seoul Songpa-gu
Korea, Republic of Samsung Medical Center Seoul
Korea, Republic of Seoul National University Hospital Seoul
Korea, Republic of Severance Hospital Seoul
Korea, Republic of The Catholic University of Korea Seoul St. Mary's Hospital Seoul
Korea, Republic of The Catholic University of Korea, Yeouido St. Mary's Hospital Seoul
Korea, Republic of Seoul National University Bundang hospital Sungnam
Korea, Republic of Ajou University Hospital Suwon

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 composite event all-cause death, myocardiac infarction, revascularization 10 years