Pounce™ Thrombectomy System Retrospective Registry

Purpose

The PROWL registry is an open-label retrospective, multi-center, US study of the Surmodics™ Pounce™ Thrombectomy System for the non-surgical removal of emboli and thrombi in the peripheral arterial vasculature.

Conditions

  • Peripheral Arterial Disease
  • Acute Limb Ischemia

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Subject underwent an endovascular intervention where the Pounce Thrombectomy System was attempted - Subject is willing and able to provide informed consent prior to the collection of study data or a consent waiver is in place

Exclusion Criteria

  • Subject is under the age of 18 years

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Arm Groups

ArmDescriptionAssigned Intervention
Retrospective All subjects in whom the Pounce Thrombectomy System was attempted will be included.
  • Device: Pounce Thrombectomy System
    Non-surgical removal of thrombi and emboli from the peripheral arterial vasculature with the Pounce Thrombectomy System.
    Other names:
    • Mechanical thrombectomy

Recruiting Locations

Vanderbilt University Medical Center
Nashville, Tennessee 37212

More Details

Status
Recruiting
Sponsor
SurModics, Inc.

Study Contact

Clinical Program Manager
1-866-787-6639
PROWLRegistry@surmodics.com

For general questions about clinical trials, contact Research Support Services at (615) 322-7343 or research.support.services@vumc.org