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)


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



Irina Stipek, CRC

Phone: 425.732.5959



Clinical Trial Categories

Vascular / Surgical

View all hospital services

Make a gift

Need urgent care?