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RECRUITING
NCT07147569

TAMBE Japan Post-Marketing Surveillance

Sponsor: W.L.Gore & Associates

View on ClinicalTrials.gov

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.

Official title: GORE® EXCLUDER® Thoracoabdominal Branch Endoprosthesis Post-Marketing Surveillance

Key Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

100

Start Date

2026-03-01

Completion Date

2034-02-28

Last Updated

2026-02-18

Healthy Volunteers

No

Interventions

DEVICE

GORE® EXCLUDER® Thoracoabdominal Branch Endoprosthesis

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)

The Jikei University Hospital

Minatoku, Japan