Trials / Not Yet Recruiting
Not Yet RecruitingNCT07480395
Real-World Data Collection of the GORE Devices When Used in the Treatment of Aortic Pathologies Which Requires the Incorporation of the Visceral Arteries.
- Status
- Not Yet Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 400 (estimated)
- Sponsor
- W.L.Gore & Associates · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
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
Detailed description
Patients are eligible to participate in the registry if at least one BXB device is intended to be incorporated (first proximal, connected with aortic main body) to maintain visceral artery perfusion. There are no selection criteria (i.e., inclusion or exclusion criteria) based on main aortic body device used, and to allow better RWD representation of the patient population treated with different aortic component, a cap per main aortic body device has been set
Conditions
- Complex Aortic Aneurysms
- Thoracoabdominal Aneurysm
- Fenestrated Endovascular Aortic Repair
- Endovascular Aortic Repair
- Abdominal Aorta Aneurism
Timeline
- Start date
- 2026-12-01
- Primary completion
- 2031-12-01
- Completion
- 2035-12-01
- First posted
- 2026-03-18
- Last updated
- 2026-03-18
Source: ClinicalTrials.gov record NCT07480395. Inclusion in this directory is not an endorsement.