NCT04229563View on ClinicalTrials.gov

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

UnknownOBSERVATIONAL
Enrollment

104

Participants

Timeline

Start Date

August 4, 2020

Primary Completion Date

March 17, 2021

Study Completion Date

April 17, 2023

Conditions
Infrainguinal Peripheral Artery DiseasePeripheral Arterial DiseasePAD
Interventions
DEVICE

AURYON™ System

"The AURYON™ System consists of two sub-units: 1) a single use catheter (AURYON™ catheter); and 2) a laser system."

Trial Locations (5)

33837

Comprehensive Cardiovascular, Davenport

52803

Midwest Cardio. research foundation, Davenport

78130

Hurricane Cardiology, New Braunfels

85259

Pulse Cardiovacular, Scottsdale

85718

Pima Vascular, Tucson

Sponsors
All Listed Sponsors
lead

Angiodynamics, Inc.

INDUSTRY

NCT04229563 - Post-Market Registry of AURYON™ Atherectomy Device in Subjects Affected With Infrainguinal Peripheral Artery Disease | Biotech Hunter | Biotech Hunter