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.
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.