Status: Recruiting
TBE Zone 2 PMS in Japan
The goal of this surveillance is to confirm the TBE device's safety and efficacy in patients treated with proximal landing in Zone 2 in the post-marketing period.
Participants needed: 200
Trial details
Biological sex: AllType: ObservationalSponsor: W.L.Gore & AssociatesUpdated: Feb 5, 2026Locations: 1Duration: 60 Months
Eligibility criteria
Those who are suitable for use of TBE according to the Japan package insert. [+3]
N/A