Digital Twin and Ml-basEd MOdel of TEVAR Interventions
Sponsor: Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Trial Details
| Condition | Aorta Disease, Aorta, Thoracic Pathologies |
| Status | Recruiting |
| Participants | 5,000 |
| Est. Completion | 30 Sept 2026 |
| Last Updated | 11 June 2026 |
Primary Outcome
Determine the accuracy of patient-specific numerical simulations in replicating TEVAR deployment outcomes
Eligibility Criteria
Inclusion Criteria
Inclusion Criteria: * ≥18 Years and older (Adult, Older Adult) * Female and male * Received TEVAR for: Chronic or acute dissection, Aneurysm, Penetrating aortic ulcer, aortic thrombus, intramural hematoma or traumatic injury Exclusion Criteria: * Younger than 18 years old * Received TEVAR in surgical graft that replaced native aorta * Poor CT image quality that leads to failure in generating a high-fidelity 3D FE model of patient anatomy (no preoperative multidetector contrast-enhanced CT-scan available, preoperative CTscan slice thickness greater than 1mm, preoperative CT-scan with artifacts, motion artifacts due to the presence of other implanted devices affecting the region of interest)
Trial Sites
Countries
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