Clinical Trials & Investigational Devices
Because FDA-approved fenestrated and branched stent-grafts remain limited, the Center provides access to next-generation devices through physician-sponsored investigational device exemption (IDE) studies.
Current studies
FDA G130266
Manufactured patient-specific and off-the-shelf fenestrated-branched stent-grafts for complex AAAs, TAAAs, and arch aneurysms. Led by Dr. Gustavo Oderich; more than 600 patients enrolled.
FDA G240006
Physician-modified endovascular grafts (PMEGs) for patients who don’t qualify for manufactured devices. Led by Dr. Steve Maximus.
Grants & funding
Federally and industry-funded research advancing complex aortic care.
Evaluating Next-Generation Fenestrated Endografts
Evaluating Next-Generation Fenestrated Endografts
A multi-year program focused on device performance, complex anatomy planning, and real-world durability in advanced aortic repair.
Computational Modeling for Complex Disease Progression
Computational Modeling for Complex Disease Progression
This initiative supports advanced modeling and simulation work to better understand progression patterns and improve procedural planning.
Ask whether a trial is right for you
Eligibility depends on your anatomy and history. Our team can review your case and discuss investigational options.