- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05380622
CHART Study of Coronary CT Angiography in Coronary Artery Disease (CHART-VISION)
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:
- 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
- To explore the precursors of plaques leading to acute coronary syndrome (ACS) or chronic coronary syndrome (CCS) in deferred coronary lesions
- 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
- 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
Conditions
Intervention / Treatment
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
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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-
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Shanghai, China
- Recruiting
- Shanghai Zhongshan Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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
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
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CHART-20220510
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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