Vanderbilt Clinical Trials

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

Arm	Description	Assigned 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

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.