Perfusion CT Registry (Perfusion CT)

March 21, 2023 updated by: Young-Hak Kim, MD, PhD
The purpose of this study is to determine whether coronary perfusion computed tomography is effective in the treatment of coronary artery disease.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

1059

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Korea, Republic of
      • Anyang, Korea, Republic of
        • Hallym University Sacred Heart Hospital
      • Bucheon, Korea, Republic of
        • Soonchunhyang University Hospital
      • Busan, Korea, Republic of
        • Dong-A University Hospital
      • Daegu, Korea, Republic of
        • Kyungpook National University Hospital
      • Daejeon, Korea, Republic of
        • The Catholic University of Korea, Daejeon St. Mary's Hospital
      • Daejeon, Korea, Republic of
        • Chungnam National University Hospital
      • Gwangju, Korea, Republic of
        • Chonnam National University Hospital
      • Jeonju, Korea, Republic of
        • Chonbuk National University Hospital
      • Pusan, Korea, Republic of
        • Pusan National University Hospital
      • Pusan, Korea, Republic of
        • Inje University Pusan Paik Hospital
      • Pusan, Korea, Republic of
        • Pusan National University Yangsan Hospital
      • Ulsan, Korea, Republic of
        • Ulsan University Hospital
    • Songpa-Gu
      • Seoul, Songpa-Gu, Korea, Republic of
        • Asan Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

General hospital

Description

Inclusion Criteria:

  • age greater than or equal to 20
  • Patient who has a coronary perfusion computed tomography

Exclusion Criteria:

  • Unwillingness or inability to give informed consent

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Only
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Accuracy of coronary perfusion computed tomography
Time Frame: 5year
Positive predictive value Negative predictive value Sensitivity Specificity
5year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Relationship between coronary perfusion computed tomography and fraction flow reserve
Time Frame: 5year
5year
Relationship between coronary perfusion computed tomography and SPECT(nuclear imaging)
Time Frame: 5year
5year
occurrence of the event after coronary perfusion computed tomography
Time Frame: 5year
Death Myocardial infarction coronary angiography Revascularization
5year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Young-Hak Kim, MD, PhD

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 22, 2013

Primary Completion (Actual)

November 25, 2020

Study Completion (Actual)

January 14, 2021

Study Registration Dates

First Submitted

September 26, 2012

First Submitted That Met QC Criteria

September 26, 2012

First Posted (Estimate)

September 28, 2012

Study Record Updates

Last Update Posted (Actual)

March 22, 2023

Last Update Submitted That Met QC Criteria

March 21, 2023

Last Verified

March 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • AMCCV 2012-04

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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