Pounce™ Thrombectomy System Retrospective Registry (PROWL)

Surmodics

Status: Enrolling

Conditions: Peripheral Arterial Disease; Acute Limb Ischemia

Treatments: Device: Pounce Thrombectomy System

Study type: Observational

Funder types: Industry

Identifiers

NCT05868161

SUR22-001

Details and patient eligibility

About

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.

Enrollment: 500 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

500 participants in 1 patient group

Retrospective

Description:

All subjects in whom the Pounce Thrombectomy System was attempted will be included.

Treatment:

Device: Pounce Thrombectomy System