Trials / Completed
CompletedNCT02373852
PMS Retrospective Study of WIRION Performance in Patients Undergoing Saphenous Vein Graft (SVG) Intervention
Post Marketing Surveillance (PMS) Retrospective Study of WIRION Performance in Patients Undergoing Saphenous Vein Graft (SVG) Intervention
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 12 (actual)
- Sponsor
- Gardia Medical · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to collect data on the use of the WIRION system in Patients undergoing Percutaneous Intervention of Saphenous Vein Graft (SVG).
Detailed description
WIRION system is used as protection device in patients undergoing SVG stenting procedure. This retrospective study collects data on the usability of the WIRION during the procedure.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Saphenous vein graft (SVG) stenting | Opening and stenting of blocked SVG with the use of the WIRION embolic protection filter |
Timeline
- Start date
- 2014-10-01
- Primary completion
- 2015-05-01
- Completion
- 2016-06-01
- First posted
- 2015-02-27
- Last updated
- 2019-09-12
- Results posted
- 2019-09-12
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT02373852. Inclusion in this directory is not an endorsement.