Characterization of Mid-term Post Market Clinical Follow Up of GORE® TAG® Thoracic Branch Endoprosthesis Facilitated Aortic Arch and Descending Aorta Intervention
Status: Recruiting
Location: See all (20) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY
The goal of this observational study is to collect mid-term post-market clinical follow-up data of GORE® TAG® Thoracic Branch Endoprosthesis used according to the standard medical practice in patients presenting with vascular disease. This registry aims to answer questions related to the efficacy and safety of GORE® TAG® Thoracic Branch Endoprosthesis.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Patient or legally authorized representative (LAR) provides written authorization and/or consent per institution and geographical requirements Patient has been or is intended to be treated with an eligible registry device Patient is age ≥ 18 years at time of informed consent signature.
Locations
Other Locations
Austria
Medizinische Universität Wien
RECRUITING
Vienna
Denmark
Rigshospitalet University Hospital
RECRUITING
Copenhagen
Germany
Universitätsklinikum Carl Gustav Carus Dresden
SUSPENDED
Dresden
University of Heidelberg
ACTIVE_NOT_RECRUITING
Heidelberg
Universitätsklinikum Schleswig-Holstein
NOT_YET_RECRUITING
Kiel
Universitätsklinikum Münster
ACTIVE_NOT_RECRUITING
Münster
Greece
Evangelismos General Hospital
RECRUITING
Athens
Laiko General hospital of Athens
ACTIVE_NOT_RECRUITING
Athens
Italy
Policlinico di Sant'Orsola
ACTIVE_NOT_RECRUITING
Bologna
ASST Spedali Civili di Brescia
RECRUITING
Brescia
IRCCS Ospedale Policlinico San Martino
RECRUITING
Genova
AOU Padova
NOT_YET_RECRUITING
Padua
Azienda Ospedaliera G. Brotzu
NOT_YET_RECRUITING
Selargius
Netherlands
Amsterdam UMC
RECRUITING
Amsterdam
Radboud UMC
RECRUITING
Nijmegen
Spain
Complejo Hospitalario Universitario de Vigo
WITHDRAWN
Vigo
Hospital Universitario Miguel Servet
ACTIVE_NOT_RECRUITING
Zaragoza
Sweden
Skane University Hospital
ACTIVE_NOT_RECRUITING
Malmo
United Kingdom
St Mary's Hospital
NOT_YET_RECRUITING
London
St Thomas' Hospital
NOT_YET_RECRUITING
London
Contact Information
Primary
Gabrielle Valle Diekmann
gvalledi@wlgore.com
+49 (0)174 690 0619
Backup
Daniele Frangioni
dfrangio@wlgore.com
+393427736782
Time Frame
Start Date: 2025-02-20
Estimated Completion Date: 2031-04
Participants
Target number of participants: 200
Treatments
GORE® TAG® Thoracic Branch Endoprosthesis
Patients treated with the TBE Device
Related Therapeutic Areas
Sponsors
Leads: W.L.Gore & Associates