Trials / Active Not Recruiting
Active Not RecruitingNCT03720704
Post-Market Registry of the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis Implanted in Peripheral Vessels
- Status
- Active Not Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 280 (actual)
- Sponsor
- W.L.Gore & Associates · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The primary objective of the VBX 17-04 registry is to collect post-market safety and performance data of the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis (VBX Stent Graft) in peripheral vessels in patients who require interventional treatment
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | GORE VIABAHN VBX Balloon Expandable Endoprosthesis | GORE VIABAHN VBX Balloon Expandable Endoprosthesis will be implanted in peripheral vessels in patients who require interventional treatment. |
Timeline
- Start date
- 2018-12-18
- Primary completion
- 2022-04-13
- Completion
- 2027-07-01
- First posted
- 2018-10-25
- Last updated
- 2026-04-14
- Results posted
- 2024-02-16
Locations
11 sites across 5 countries: France, Germany, Italy, Netherlands, Spain
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03720704. Inclusion in this directory is not an endorsement.