CHART Study of Coronary CT Angiography in Coronary Artery Disease (CHART-VISION)

May 18, 2022 updated by: Shanghai Zhongshan Hospital

CHART Study of Coronary CT Angiography to Predict Imaging and Cardiovascular Outcomes in Patients With Coronary Artery Disease

In a cohort of patients referred to coronary computed tomography angiography (CCTA), the investigators aim:

  1. To describe the natural history of the coronary atherosclerotic plaque development and progression or regression, as well as the plaque characterization and phenotypes over time by CCTA among deferred coronary lesions
  2. To explore the precursors of plaques leading to acute coronary syndrome (ACS) or chronic coronary syndrome (CCS) in deferred coronary lesions
  3. To investigate prognostic implication of qualitative and quantitative plaque analysis of stenosis and plaque features, disease patterns, hemodynamic parameters, and fat metrics on CCTA along with physiologic assessment
  4. To investigate the effects of different treatment strategies according to stenosis and plaque features, fat metrics on CCTA along with physiologic assessments.

Study Overview

Status

Recruiting

Detailed Description

Invasive physiologic indices such as fractional flow reserve (FFR) are used to define ischemia-causing stenosis and guide percutaneous coronary intervention (PCI) in the clinical practice. FFR-guided PCI has been proven to improve clinical outcomes, however, a substantial proportion of patients continue to experience clinical events. The ISCHEMIA trial showed that invasive therapy did not improve prognosis in patients with moderate to severe ischemia compared to optimal medical therapy. Besides, a recent study implied that even in vessels with FFR>0.80, those have lesions with high-risk plaque characteristics (HRPC) demonstrated worse clinical outcomes. This might be not unexpected since previous evidence from postmortem studies demonstrated that unstable atherosclerotic plaques are prone to rupture and trigger adverse cardiovascular events.

In recent years, advances in imaging analysis made it possible to conduct novel measurements such as pericoronary inflammation or epicardial fat metrics and lesion-specific or vessel-specific hemodynamic parameters derived from CCTA (such as fractional flow reserve by CCTA [CT-FFR]) as well as the coronary disease patterns defined by physiologic distribution (predominant focal versus diffuse disease defined by CCTA derived pullback pressure gradient index) and local severity (presence versus absence of major gradient defined by CCTA-derived FFR gradient per unit length [dCT-FFR/ds]) of coronary atherosclerosis.

However, the relationship of these parameters and the combination of these indices on clinical outcomes has not been fully understood. Furthermore, though it has been known that high-risk plaques are related with worse outcomes even no significant blood flow impairment induced, best treatment strategy for these lesions remains unclear.

In this regard, the aims of this study are multiple, all the treatment strategies are at the discretion of the physicians in charge. For patients without further invasive angiography performed after CCTA or deferred for revascularization after invasive angiography with/without physiology or imaging assessments, the investigators will investigate coronary atherosclerotic plaque development and progression or regression, as well as the plaque characterization and phenotypes over time by CCTA, and to explore the precursors of plaques leading to acute coronary syndrome (ACS) or chronic coronary syndrome (CCS); for those with received revascularization, the investigators will investigate the prognostic value of CCTA based comprehensive analysis of coronary in combination with physiologic assessment. In all patients, the effects of different treatment strategies according to stenosis and plaque features, fat metrics as well as physiologic assessments will be investigated.

CHART is a study group called Chinese Non-invasive Cardiovascular Imaging and Physiology Study Group, the current study will be conducted by CHART and by invitation in multiple Chinese centers.

Study Type

Observational

Enrollment (Anticipated)

5000

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

      • Shanghai, China
        • Recruiting
        • Shanghai Zhongshan Hospital

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients with an indication for CCTA.

Description

Inclusion Criteria:

  • Patients with an indication for CCTA.
  • Qualified patients who have signed a written informed consent form.

Exclusion Criteria:

  • Left ventricular ejection fraction < 35%
  • Acute ST-elevation myocardial infarction within 72 hours or previous coronary artery bypass graft surgery
  • Abnormal epicardial coronary flow (TIMI flow < 3)
  • Planned coronary artery bypass graft surgery after diagnostic angiography
  • Poor quality of CCTA or other reasons by core lab that are unsuitable for plaque, physiological or fat analysis
  • Patients with a stent in the target vessel

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Without ICA or deferral of PCI after ICA group
Patients didn't undergo invasive coronary angiography (ICA) or with a vessel determined to defer revascularization.

Coronary CT angiography (CCTA) will be performed according to standard protocol and measurement of fractional flow reserve (FFR) or other physiological indices will be at the at the discretion of the physicians in charge.

Stenosis and plaque features, disease patterns, hemodynamic parameters, and fat metrics on CCTA will be analyzed blindly in the core lab.

PCI group
Patients with a vessel that undergo percutaneous coronary intervention (PCI)

Coronary CT angiography (CCTA) will be performed according to standard protocol and measurement of fractional flow reserve (FFR) or other physiological indices will be at the at the discretion of the physicians in charge.

Stenosis and plaque features, disease patterns, hemodynamic parameters, and fat metrics on CCTA will be analyzed blindly in the core lab.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Frequency of occurrence of high-risk plaques
Time Frame: 30 days
Frequency (%) of occurrence of high-risk plaque morphologic features (Housfield Unit[HU]<30, Remodelling Index > 1.1, napkin-ring sign, spotty calcium, minimal lumen area[MLA]<4mm2 & plaque burden[PB]≥70%), physiologic diffuse disease, inflammation by high fat attenuation index (FAI)
30 days
Change in total plaque volume (adjusted by vessel volume) and plaque composition detected by follow up CCTA
Time Frame: up to 5 years after index procedure
Change in total plaque volume (adjusted by vessel volume) and plaque composition detected by follow up CCTA
up to 5 years after index procedure
Change in WSS detected by follow up CCTA
Time Frame: up to 5 years after index procedure
Change in hemodynamic parameter of wall shear stress (WSS) detected by follow up CCTA
up to 5 years after index procedure
Change in APS detected by follow up CCTA
Time Frame: up to 5 years after index procedure
Change in hemodynamic parameter of axial plaque stress (APS) detected by follow up CCTA
up to 5 years after index procedure
Change in SSI detected by follow up CCTA
Time Frame: up to 5 years after index procedure
Change in stenosis susceptibility index (SSI) detected by follow up CCTA
up to 5 years after index procedure
Change in hemodynamic parameters delta fractional flow reserve detected by follow up CCTA
Time Frame: up to 5 years after index procedure
Change in hemodynamic parameters delta fractional flow reserve detected by follow up CCTA
up to 5 years after index procedure
Change in physiological pattern by PPG derived by follow up CCTA
Time Frame: up to 5 years after index procedure
Change in physiological pattern by pullback pressure gradient (PPG) derived by follow up CCTA
up to 5 years after index procedure
Change in dCT-FFR/ds detected by follow up CCTA
Time Frame: up to 5 years after index procedure
Change in dCT-FFR/ds detected by follow up CCTA
up to 5 years after index procedure
Change in CT-FFR
Time Frame: up to 5 years after index procedure
Change in fractional flow reserve by CCTA
up to 5 years after index procedure
Change in peri-coronary adipose tissue assessed by follow up CCTA
Time Frame: up to 5 years after index procedure
Change in peri-coronary adipose tissue assessed by follow up CCTA
up to 5 years after index procedure
CCTA-derived features associated with precursors of ACS or CCS
Time Frame: up to 5 years after index procedure
CCTA-derived features associated with precursors of ACS or CCS
up to 5 years after index procedure
Adverse cardiovascular event according to stenosis and plaque features, disease patterns, hemodynamic parameters, and fat metrics on CCTA along with physiologic assessment
Time Frame: up to 5 years after index procedure
A composite of cardiac death, vessel-related myocardial infarction (MI), or vessel-related ischemia-driven revascularization.
up to 5 years after index procedure
Adverse cardiovascular event according to different treatment strategies according to stenosis and plaque features, fat metrics on CCTA along with physiologic assessments.
Time Frame: up to 5 years after index procedure
A composite of cardiac death, vessel-related myocardial infarction (MI), or vessel-related ischemia-driven revascularization.
up to 5 years after index procedure

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Anginal status
Time Frame: up to 5 years after index procedure
Change in Health Related Quality of Life (HRQL)
up to 5 years after index procedure
Number of anti-anginal medication prescribed
Time Frame: up to 5 years after index procedure
Number of anti-anginal medication prescribed
up to 5 years after index procedure
Clinical predictors of events
Time Frame: up to 5 years after index procedure
To find out the models with baseline characteristics including age, sex, cardiovascular risk factors and so on with the highest area under curve to predict a composite of cardiac death, vessel-related myocardial infarction (MI), or vessel-related ischemia-driven revascularization.
up to 5 years after index procedure
Prognostic value of CCTA defined anatomy and plaque characterization
Time Frame: up to 5 years after index procedure
Prognostic value of CCTA defined anatomy including diameter stenosis, area stenosis and plaque characterization including plaque components, physiological on blood flow, diffuseness and inflammation.
up to 5 years after index procedure
Prognostic value of WSS
Time Frame: up to 5 years after index procedure
Prognostic value of WSS
up to 5 years after index procedure
Prognostic value of APS
Time Frame: up to 5 years after index procedure
Prognostic value of APS
up to 5 years after index procedure
Prognostic value of SSI
Time Frame: up to 5 years after index procedure
Prognostic value of SSI
up to 5 years after index procedure
Prognostic value of delta CT-FFR
Time Frame: up to 5 years after index procedure
Prognostic value of delta CT-FFR
up to 5 years after index procedure
Prognostic value of pull pressure gradient
Time Frame: up to 5 years after index procedure
Prognostic value of pull pressure gradient
up to 5 years after index procedure
Prognostic value of dCT-FFR/ds
Time Frame: up to 5 years after index procedure
Prognostic value of dCT-FFR/ds
up to 5 years after index procedure
Prognostic value of per-coronary adipose tissue
Time Frame: up to 5 years after index procedure
Prognostic value of per-coronary adipose tissue derived fat attenuation index and other radiomics features.
up to 5 years after index procedure
Prognostic value of integrated CCTA based lesion anatomy, plaque characterization, hemodynamic parameters, physiological patterns and per-coronary adipose tissue for ACS
Time Frame: up to 5 years after index procedure
Comparison of outcome discrimination ability.
up to 5 years after index procedure
Prognostic value of integrated CCTA based lesion anatomy, plaque characterization, hemodynamic parameters, physiological patterns and per-coronary adipose tissue for cardiovascular events
Time Frame: up to 5 years after index procedure
Comparison of outcome discrimination ability.
up to 5 years after index procedure
Relationship among CT-derived plaque qualification and quantification, and CT-defined pericoronary and epicardial fat metrics with physiological assessments.
Time Frame: up to 5 years after index procedure
Association among CCTA parameters (including diameter stenosis, area stenosis, plaque components) and physiologic indices (CT-FFR, PPG, delta-FFR, dCT-FFR/ds).
up to 5 years after index procedure

Collaborators and Investigators

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

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)

January 1, 2015

Primary Completion (Anticipated)

December 31, 2025

Study Completion (Anticipated)

December 31, 2030

Study Registration Dates

First Submitted

May 10, 2022

First Submitted That Met QC Criteria

May 13, 2022

First Posted (Actual)

May 19, 2022

Study Record Updates

Last Update Posted (Actual)

May 25, 2022

Last Update Submitted That Met QC Criteria

May 18, 2022

Last Verified

May 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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