RecruitingNCT05777460
Mid- and Long-term Outcomes of Custom-made Aortic Devices
Results From a Multicenter Registry on the Outcomes of the Terumo Custom-made Aortic Endograft
Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Enrollment
60 participants
Start Date
Oct 1, 2020
Study Type
OBSERVATIONAL
Conditions
Summary
This study aims to evaluate mid- and long-term outcomes after Thoracic endovascular aortic repair (TEVAR) with custom-made devices.
Eligibility
Min Age: 18 Years
Inclusion Criteria1
- Thoracic Aortic Disease
Exclusion Criteria1
- Urgent/Emergent treatment
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
DEVICEThoracic endovascular aortic repair (TEVAR)
The TEVAR procedure involves the placement of a covered stent (a metal mesh tube with a layer of fabric) into the weakened area of the artery.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT05777460
Related Trials
Intervascular Post-Market Clinical Follow-Up (PMCF) Registry
NCT073229134 locations
Impact of Aortic Diseases on Quality of Life and Work Ability
NCT074791861 location
HEART: Pilot Randomized Controlled Trial
NCT074831771 location
Incidence of Major Complication in Case of Thoracic Aortic Aneurysm
NCT053955981 location
Development of CIRC Technologies
NCT056542721 location