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High Performance Computing of Personalized Cardio Component Models

High Performance Computing of Personalized Cardio Component Models

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02235883
Acronym
HEART
Enrollment
94
Registered
2014-09-10
Start date
2014-08-31
Completion date
2017-01-31
Last updated
2018-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease

Keywords

Coronary artery disease, FFR, diagnosis, computational model, non-invasive

Brief summary

The objective of the HEART Study is to develop a multiscale model of the coronary circulation based on multimodal imaging data (angiography, echocardiography). The predictive comprehensive multi-scale model, developed during this proof-of-concept study, will be used for analyzing functional aspects of coronary artery disease. Model validation is performed against invasive measurements

Detailed description

The main objective of HEART is the development and validation of a patient-specific multiscale computational model of the coronary circulation with high predictive power in healthy and diseased vessels: * Comprehensive modeling of the anatomical and hemodynamic phenomena in the coronary circulation based on input data acquired from both angiography and echocardiography; * Assessment of functional parameters and subsequent validation of the models; * High performance computing architecture for efficiently addressing the multi-scale complexity, which is a critical requirement for translation into clinical decision making. Patient measurements used as input data for the multiscale models, or for validating the computational results include: * Angiography: targeted angiographic views include LAO 30, LAO 30/20 cranial, LAO 30/20 caudal, RAO 30 (RCA views) and RAO 25/25 caudal, RAO 0/40 caudal, RAO 10/40 cranial, LAO 50/20 cranial, LAO 50/20 caudal (LCA views) * Echocardiography: * Standard apical acquisitions (2D harmonic 4-chamber, 2-chamber, 3-chamber) * Color flow Doppler/spectral Doppler (MR, AI, TR evaluation; CW and PW spectral Doppler) * Three-dimensional imaging (From apical 4-chamber view one ECG-triggered real time complete full volume acquisition including LV and LA - 1 acquisition at low volume per second (VPS) rate and one at high VPS, real time volumetric color flow Doppler, cover MV and AV). * Non-invasive pressure measurements: cuff-based measurements at the left and right arm, before echocardiography and angiography * Invasive pressure measurements: rest - aortic pressure (Pa), distal pressure (Pd), Pd/Pa ratio; hyperemia - aortic pressure (Pa), distal pressure (Pd), FFR (Pd/Pa)

Interventions

None listed

Sponsors

Spitalul Clinic de Urgenţǎ Bucureşti
CollaboratorUNKNOWN
Siemens Corporate Technology Romania
CollaboratorINDUSTRY
Universitatea Politehnica Bucureşti
CollaboratorUNKNOWN
Transilvania University of Brasov
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age \>18 years * providing written informed consent * scheduled to undergo clinically-indicated non-emergent invasive coronary angiography (ICA) * likelihood of stenosis in one of the main coronary epicardial vessels (LAD, LCx, RCA)

Exclusion criteria

* prior PCI * prior bypass surgery * prior valve surgery or replacement * significant arrhythmia * very low systolic BP (\<90 mmHg) * abnormally high HR (\>120 bpm) * significant Left Main disease * STEMI or NSTEMI * suspected microvascular disease

Design outcomes

Primary

MeasureTime frameDescription
Accuracy of coronary hemodynamic indices extracted from the computational model of the coronary circulation as compared to the invasively measured indices (FFR, basal Pd/Pa)up to 18 monthsCoronary hemodynamic indices (FFR, basal Pd/Pa) are measured invasively and are computed from the computational model of coronary hemodynamics. The diagnostic accuracy of the computed hemodynamic indices is evaluated against the measured hemodynamic indices.

Secondary

MeasureTime frameDescription
Net reclassification index when using echocardiography data as input parameters for the computational model (in addition to the angiographic data)up to 18 monthsCoronary hemodynamic indices (FFR, basal Pd/Pa) are determined from the computational model in two configurations: with and without echocardiography based input data. We evaluate the net reclassification index of the computed coronary hemodynamic indices when echocardiography based input data is used (as compared to the gold standard represented by the measured coronary hemodynamic indices).
Numerical correlation between computed and measured distal coronary pressure at rest and hyperemiaup to 18 monthsDistal coronary pressure at rest and hyperemia are measured invasively and are extracted from the computational model. The correlation between measured and computed quantities is evaluated.

Countries

Romania

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026