TAMBE Japan Post-Marketing Surveillance
GORE® EXCLUDER® Thoracoabdominal Branch Endoprosthesis Post-Marketing Surveillance
W.L.Gore & Associates
100 participants
Mar 1, 2026
OBSERVATIONAL
Conditions
Summary
To evaluate the safety and efficacy of multi component system (TAMBE device) including GORE® EXCLUDER® Thoracoabdominal Branch Endoprosthesis (Aortic Component; AC) under post-marketing use.
Eligibility
Inclusion Criteria3
- Patients who were attempted to implant the AC
- Thoracoabdominal aortic aneurysm
- Pararenal abdominal aortic aneurysm
Exclusion Criteria1
- N/A
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Interventions
The target patients are those who were attempted to implant the AC during the enrollment period of this surveillance. Patients will also be targeted even if all components of the TAMBE device (devices that can be used in combination with AC specified in IFU) were not used, or if a device other than the component of the TAMBE device was used.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07147569