MedTrace Logo

Pounce™ Thrombectomy System Retrospective Registry

NCT05868161 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2025-09-11

No results posted yet for this study

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.

Conditions

  • Peripheral Arterial Disease
  • Acute Limb Ischemia

Interventions

DEVICE

Pounce Thrombectomy System

Non-surgical removal of thrombi and emboli from the peripheral arterial vasculature with the Pounce Thrombectomy System.

Sponsors & Collaborators

  • SurModics, Inc.

    lead INDUSTRY

Principal Investigators

  • Sean Lyden, MD · The Cleveland Clinic

  • Joseph Campbell, MD · OhioHealth

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-04-18
Primary Completion
2026-05-31
Completion
2026-07-31
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05868161 on ClinicalTrials.gov