The full title of this study is: VIRTUS: Safety and Efficacy of the Veniti Vici™Venous Stent System when Used to Treat Clinically Significant Chronic Non-malignant Obstruction of the Iliofemoral Venous Segment
The VIRTUS study evaluates the Veniti Vici™ Venous Stent System in patients whose doctor has determined that blood-flow through a vein in their leg has been restricted. The Veniti Vici™ Venous Stent System will be assessed on those who have a presence of unilateral, clinically significant, chronic non-malignant obstruction of the common femoral vein, external iliac vein, common iliac vein, or any combination thereof, defined as a ≥50% reduction in target vessel lumen diameter. The information gathered will help assess the safety and efficacy of the investigational stent system.
Principal Investigator: Peter Stratil, MD, MBA
For more information about this trial, please contact Alicia Drew, Director, Research and Physician Services at Radiology Imaging Associates.
If you would like to explore more clinical information about this trial, please see the trial page on ClinicalTrials.gov