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

    1. All causes mortality [6month, each year]

    2. Cardiac death [6 month, each year]

    3. Myocardial infarction [6 month, each year]

    4. target lesion revascularization [6 month, each year]

    5. target vessel revascularization [6 month, each year]

    Secondary Outcome Measures

    1. non target vessel revascularization [6 month, each year]

    2. Stent thrombosis [6 month, each year]

    3. Serum databank for evaluation of biomarkers outcomes [6 month, each year]

    4. 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:

    Study Results

    No Results Posted as of Aug 5, 2020