Pounce™ Thrombectomy System Retrospective Registry

Status: Recruiting
Location: See all (9) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY

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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
United States
Illinois
OSF St. Francis Medical Center
RECRUITING
Peoria
Indiana
Community Hospital
COMPLETED
Munster
Louisiana
Baton Rouge General Medical Center
RECRUITING
Baton Rouge
Minnesota
Allina Health
COMPLETED
Minneapolis
Ohio
Cleveland Clinic
RECRUITING
Cleveland
South Carolina
Prisma Health Upstate
RECRUITING
Greenville
South Dakota
North Central Heart
RECRUITING
Sioux Falls
Tennessee
Vanderbilt University Medical Center
RECRUITING
Nashville
Texas
Ascension Seton
RECRUITING
Austin
Contact Information
Primary
Clinical Program Manager
PROWLRegistry@surmodics.com
1-866-787-6639
Time Frame
Start Date: 2023-04-18
Estimated Completion Date: 2026-07-31
Participants
Target number of participants: 500
Treatments
Retrospective
All subjects in whom the Pounce Thrombectomy System was attempted will be included.
Sponsors
Leads: SurModics, Inc.

This content was sourced from clinicaltrials.gov

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