CathOlic Medical Center percutAneous Coronary inTervention Registry (COACT)
Sponsor
The Catholic University of Korea (Other)
Overall Status
Completed
CT.gov ID
NCT01239914
Collaborator
Seoul St. Mary's Hospital (Other), Yeouido St. Mary's Hospital (Other), Bucheon St. Mary's Hospital (Other), St.Paul's Hospital, Korea (Other), Incheon St.Mary's Hospital (Other), Saint Vincent's Hospital, Korea (Other), Daejeon St. Mary's hospital (Other)
11,719
8
179
1464.9
8.2
Study Details
Study Description
Brief Summary
COACT registry is a multicenter registry of consecutive patients undergoing coronary stent implantation at 8 centers in the Catholic University of Korea to evaluate the real world management of patients with coronary artery disease and to assess their in-hospital, medium and long-term outcomes.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Study Design
Study Type:
Observational
Actual Enrollment
:
11719 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
CathOlic Medical Center percutAneous Coronary inTervention Registry (COACT)
Study Start Date
:
Jan 1, 2005
Actual Primary Completion Date
:
Dec 1, 2019
Actual Study Completion Date
:
Dec 1, 2019
Outcome Measures
Primary Outcome Measures
- All causes mortality [6month, each year]
- Cardiac death [6 month, each year]
- Myocardial infarction [6 month, each year]
- target lesion revascularization [6 month, each year]
- target vessel revascularization [6 month, each year]
Secondary Outcome Measures
- non target vessel revascularization [6 month, each year]
- Stent thrombosis [6 month, each year]
- Serum databank for evaluation of biomarkers outcomes [6 month, each year]
- Pharmacogenetic and cardiovascular genetic studies associated to clinical outcomes [6 month, each year]
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
-
all consecutive patients who underwent percutaneous coronary intervention
-
written informed consent for the DNA and serum databank
Exclusion Criteria:
- patients who did not agreed to participate
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Bucheon St.Mary Hospital | Bucheon | Gyeonggido | Korea, Republic of | |
2 | St.Vincent's Hospital | Suwon | Gyeonggido | Korea, Republic of | |
3 | Uijeongbu St.Mary's Hospital | Uijeongbu | Gyeonggido | Korea, Republic of | |
4 | Daejeon St.Mary's Hospital | Daejeon | Korea, Republic of | ||
5 | Incheon St.Mary's Hospital | Incheon | Korea, Republic of | ||
6 | Seoul St.Mary's Hospital | Seoul | Korea, Republic of | 137-701 | |
7 | St.Paul's Hospital | Seoul | Korea, Republic of | ||
8 | Yeouido St.Mary Hospital | Seoul | Korea, Republic of |
Sponsors and Collaborators
- The Catholic University of Korea
- Seoul St. Mary's Hospital
- Yeouido St. Mary's Hospital
- Bucheon St. Mary's Hospital
- St.Paul's Hospital, Korea
- Incheon St.Mary's Hospital
- Saint Vincent's Hospital, Korea
- Daejeon St. Mary's hospital
Investigators
- Study Chair: Ki-Bae Seung, M.D.,PhD, Seoul St. Mary's Hospital
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Kiyuk Chang, MD,PhD,
Professor,
The Catholic University of Korea
ClinicalTrials.gov Identifier:
NCT01239914
Other Study ID Numbers:
- COACT
First Posted:
Nov 15, 2010
Last Update Posted:
Aug 5, 2020
Last Verified:
Aug 1, 2020
Keywords provided by Kiyuk Chang, MD,PhD,
Professor,
The Catholic University of Korea
Additional relevant MeSH terms: