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NCT04229563

Post-Market Registry of AURYON Atherectomy Device in Subjects Affected With Infrainguinal Peripheral Artery Disease

Sponsor: Angiodynamics, Inc.

View on ClinicalTrials.gov

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

DEVICE

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