PMS Retrospective Study of WIRION Performance in Patients Undergoing Saphenous Vein Graft (SVG) Intervention

Gardia Medical

Status: Completed

Conditions: Stenosis

Treatments: Device: Saphenous vein graft (SVG) stenting

Study type: Observational

Funder types: Industry

Identifiers

NCT02373852

SVG-CL003

Details and patient eligibility

About

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).

Full 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.

Enrollment: 12 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients underwent percutaneous intervention (PI) of SVG stenting in which the WIRIONTM system was used.
• Patient is greater than or equal to 18 years of age.

Exclusion criteria

• Undergone cardiac surgery in the past 60 days before the procedure.