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Post-Market Registry of AURYON Atherectomy Device in Subjects Affected With Infrainguinal Peripheral Artery Disease
Sponsor: Angiodynamics, Inc.
Summary
The PATHFINDER Registry is a prospective, non-randomized, single arm, multicenter observational study. This pilot registry is aimed to evaluate the performance (peri-procedural) and clinical outcomes (intermediate and long-term) of the AURYON Atherectomy System, within the initial launch phase of the product in the market.
Official title: PATHFINDER Post-Market Registry of AURYON Atherectomy Device in Subjects Affected With Infrainguinal Peripheral Artery Disease (EX-PAD-05)
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
102
Start Date
2020-08-04
Completion Date
2023-04-17
Last Updated
2026-05-18
Healthy Volunteers
No
Interventions
AURYON Atherectomy System
The AURYON Atherectomy System consists of two sub-units: 1) a single use catheter ("AURYON™ catheter"); and 2) a laser system.
Locations (10)
Pulse Cardiovacular
Scottsdale, Arizona, United States
Pima Vascular
Tucson, Arizona, United States
Comprehensive Cardiovascular
Davenport, Florida, United States
First Coast Cardiovascular Institute
Jacksonville, Florida, United States
Amavita Clinical Research
Miami, Florida, United States
Rush University Medical Center
Chicago, Illinois, United States
Midwest Cardio. research foundation
Davenport, Iowa, United States
NJ Endovascular Amputation Prevention
Clifton, New Jersey, United States
Medical City Heart and Spine
Dallas, Texas, United States
Hurricane Cardiology
New Braunfels, Texas, United States