Overview

BARD Registry Study

A Prospective, Multicenter, Single Arm, Real-World Registry Assessing the Clinical Use of the Lutonix® 035 Drug Coated Balloon Catheter in Arteries of the Superficial Femoral Artery (SFA) and Popliteal Artery (PA) (SAFE-DCB U.S. Registry)

Objective

This registry study is enrolling patients with blockages, or stenosis, in their superficial femoral artery (SFA) or popliteal artery from Lake Washington Vascular. The purpose of this patient registry is to assess the safety and usage of the Lutonix® DCB PTA catheter.

 

Study Coordinator(s)

Krissa Gunderson, CRC

Phone: 425.732.5958

krissag@lkwv.com

 

Irina Stipek, CRC

Phone: 425.732.5959

irinas@lkwv.com

 

Clinical Trial Categories

Vascular / Surgical

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