Status: Not yet recruiting
Real-World Data Collection of GORE Devices Used In the Endovascular Treatment of Aortic Aneurysms Which Incorporate Visceral Arteries.
The registry population consists of patients presenting with complex aortic pathologies amenable to endovascular aortic repair that requires the incorporation of bridging stents to maintain visceral artery perfusion
Participants needed: 400
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: W.L.Gore & AssociatesUpdated: Jun 1, 2026Duration: 5 Years
Eligibility criteria
Informed Consent Form (ICF) is signed by Subject. [+4]
Patient has a prior visceral artery stenting not associated with registry proced... [+6]