About this trial

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.

Eligibility criteria

Qualifiers

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

Disqualifiers

Subject is under the age of 18 years

Trial design

Treatments tested in this trial

  • Pounce Thrombectomy System

Treatment groups

500 Participants
are divided into 1 treatment group

Locations

9
Illinois
OSF St. Francis Medical Center61637, Peoria United States
Indiana
Community Hospital46321, Munster United States
Louisiana
Baton Rouge General Medical Center70809, Baton Rouge United States
Minnesota
Allina Health55407, Minneapolis United States

Sponsors and collaborators

SurModics, Inc.

Lead sponsor