Single-arm, non-randomized, prospective, multi-center study with the Bard® LifeStent® Vascular Stent Delivery. (BARD)

Basic data for this project

Type of projectIndividual project
Duration at the University of Münster01/08/2010 - 31/07/2013

Description

In this study the Bard® LifeStent® Vascular Stent Delivery System is used in subjects with lifestyle-limiting claudication or ischemic rest pain that are candidates for percutaneous transluminal angioplasty (PTA) and stenting with lesion(s) in the infra-inguinal segment (superficial femoral artery (SFA) and/or proximal popliteal artey). Subjects will be treated with PTA followed by implantation of the Bard® LifeStent® Vascular Stent. Clinical follow-up for all subjects will be performed prior to hospital discharge, 30 days, 12-, 24-, and 36-months post index procedure.

KeywordsKathetertechnik; Spinalballon
Funding identifierBPV-09-006
Funder / funding scheme
  • Bard Peripheral Vascular Inc. (Bard)

Project management at the University of Münster

Reinecke, Holger

Applicants from the University of Münster

Reinecke, Holger

Research associates from the University of Münster

Meyborg, Matthias