Impact of Coronary CT Angiography, Physiologic Assessment and Pharmacotherapy on the Clinical Outcomes

NCT04547231 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 992

Last updated 2021-03-23

No results posted yet for this study

Summary

The investigators aim to investigate the prognostic implication of stenosis and plaque features on coronary CT angiography (CCTA), physiologic assessment, and pharmacotherapy after invasive coronary angiography.

Conditions

Interventions

DIAGNOSTIC_TEST

Fractional flow reserve, Coronary CT angiography

1. Coronary CT angiography (CCTA) and measurement of fractional flow reserve (FFR) will be performed as part of routine clinical practice. The decision to perform CCTA before invasive angiography was at the judgment of the physicians in charge. 2. Physiologic assessment includes delta FFR (lesion-specific) and FFR (vessel-specific) measurement. Delta FFR is defined as a pressure step up across the lesion. Coronary angiography and physiologic assessment will be analyzed by an independent core laboratory (Seoul National University Hospital, Clinical Trial Center, Seoul, South Korea). 3. Stenosis and plaque features on CCTA will be analyzed by an independent CCTA core laboratory (Severance Cardiovascular Hospital, Seoul, Korea), and pericoronary and epicardial fat metrics (fat attenuation index, epicardial fat attenuation index, epicardial fat volume, etc.) will be obtained by an independent cardiac CT fat core laboratory (Tsuchiura Kyodo general hospital, Ibaraki, Japan).

Sponsors & Collaborators

  • Seoul National University Bundang Hospital

    collaborator OTHER
  • Keimyung University Dongsan Medical Center

    collaborator OTHER
  • Ulsan Hospital

    collaborator UNKNOWN
  • Inje University

    collaborator OTHER
  • Sejong General Hospital

    collaborator OTHER
  • Chosun University Hospital

    collaborator OTHER
  • Gachon University Gil Medical Center

    collaborator OTHER
  • Dong-A University Hospital

    collaborator OTHER
  • Wonju Severance Christian Hospital

    collaborator OTHER
  • Incheon St.Mary's Hospital

    collaborator OTHER
  • Tsuchiura Kyodo General Hospital

    collaborator OTHER
  • Second Affiliated Hospital, School of Medicine, Zhejiang University

    collaborator OTHER
  • Dong-A ST Co., Ltd.

    collaborator INDUSTRY
  • Seoul National University Hospital

    lead OTHER

Principal Investigators

  • Bon-Kwon Koo, MD, PhD · Seoul National University Hospital

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-08-12
Primary Completion
2024-12-31
Completion
2025-12-31

Countries

  • South Korea

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04547231 on ClinicalTrials.gov