A post-approval registry of the TREO stent-graft for patients with infrarenal abdominal aortic aneurysms

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A post-approval registry of the TREO stent-graft for patients with infrarenal abdominal aortic aneurysms Dr. Theodosios Bisdas Associate Professor for Vascular Surgery Clinic for Vascular Surgery St. Franziskus Hospital, Muenster, Germany

Disclosures Speaker name: Theodosios Bisdas I have the following potential conflicts of interest to report: X X Consulting: Other: Medtronic, Bolton Medical, COOK, Penumbra, BBraun, Bard, Boston Scientific VASCUPEDIA (Co-founder)

The challenge of registries for CEmarked devices Increasing requirements for clinical data, including post-market clinical follow-up (PMCF) from CEmarked devices Assumptions about registries are not reflected in the new regulations (new EU MDR 2017/745) Registries are being encouraged by regulatory bodies (e.g. European Medicines Agency) to allow for clinical trials to be embedded

The advantages of a registry Medical device performance in a real-world setting Large number of patients Diverse clinical settings Registries permit follow-up that can span decades Clinical Trials Transformation Initiative: Conducting Clinical Trials using Clinical Observational Registries. https://www.ctticlinicaltrials.org/projects/registry-trials

T R E O R E G I S T R Y D E S I G N This is a prospective, multicenter, post -market clinical follow-up, non-randomized registry of the TREO Stent -Graft. Subjects diagnosed with infrarenal aortic aneurysms and treated with the TREO Stent-Graft device can be included into the registry. Pre-procedure baseline data will be gathered as well as post-procedure assessments prior to hospital discharge and one to three months and 1, 2, 3, 4, and 5-year postimplantation. 5

THE TREO REGISTRY DESIGN TREO Registry is to study the use and effectiveness of the TREO Stent Graft System in the real world. In order to accomplish this goal this registry will be designed as an Open Ended and All Comers study. Start First patient in Last patient in Interim analyses 5 Year Followup Mar 2017 Jun 2017 Q1 2019 Q1 2024 6

ENDPOINTS Traditional Clinical Endpoints Device Specific Endpoints Health Economic Endpoints

TRADITIONAL CLINICAL ENDPOINTS Aneurysm Related Mortality All Cause Mortality / Aneurysm Rupture Adverse Events Conversion to Open Endoleak (Type II)

DEVICE-SPECIFIC ENDPOINTS Technical Success Endoleak (I, III) / Patency Device Integrity Migration Sac Change

HEALTH-ECONOMIC ENDPOINTS / Procedure Time Fluoro Time Contrast Blood Loss Number of Pieces Access Modality Hospital Stay ICU Time Ancillary Device

Cases in St. Franziskus Hospital Muenster, Germany Case #1 Severely calcified access vessels

Cases in St. Franziskus Hospital Muenster, Germany Case #2 Short proximal neck

TREO Registry update 600 patients First patient in Jun 2017 35 patients enrolled to date 16 sites recruiting 18 pending initiation 5-year follow-up First results to be presented in 2019

TREO registry innovations & challenges Quality by design Endpoints adhering to EVAR reporting standards Core-lab adjudication Careful assessment of safety endpoints First EVAR registry initiated under the new MDR Ethical committees expectations of pharmaceutical clinical trials being applied to an observational study with CE-marked device

TREO Registry collaborating sites Imeldaziekenhuis, Bonheiden, BE AZ Sint Blasius, Dendermonde, BE Civico, Ospedale Regionale, Lugano, CH St. Franziskus Hospital, Muenster, DE St. Bonifatius Hospital, Lingen, DE Klinikum Peine ggmbh, Peine, DE University Hospital Tübingen, Tübingen, DE Klinikum Chemnitz, Chemnitz, DE Klinikum Augsburg, Augsburg, DE University Heart Center Freiburg, DE Policlinico S. Maria Alle Scotte, Siena, IT Policlinico Tor Vergata, Roma, IT Compensorio Sanitario Bolzano, IT Ospedale San Gerardo, Monza, IT Azienda Ospedaliera di Catania, IT Ospedale San Giovanni, Roma, IT CdC Villa dei Fiori, Acerra, IT Policlinico Consorziale di Bari, IT Rijnstate Hospital, Arnhem, NL UMC Groningen, NL UMCU, Utrecht, NL Haukeland University Hospital, Bergen,NO Hospital de Santa Marta, Lisboa, PT Hospital Clínic, Barcelona, ES Complejo Hospitalario Universitario de Ourense, ES Hospital Universitario Lucus Augusti, Lugo, ES Manchester Royal Infirmary, Manchester, UK John Radcliffe, Oxford, UK Royal Hospital Liverpool, UK

A post-approval registry of the TREO stent-graft for patients with infrarenal abdominal aortic aneurysms Dr. Theodosios Bisdas Associate Professor for Vascular Surgery Clinic for Vascular Surgery St. Franziskus Hospital, Muenster, Germany