Automated Non-Invasive Arterial Pressure Device in Normals and in Patients with Peripheral Arterial Disease

Overview

About this study

The purpose of this study is to determine the accuracy of an automated non-invasive arterial pressure device when assessing people with peripheral arterial disease. The arterial pressure from each limb and calculated ABI’s from standard non-invasive arterial vascular testing verses automated non-invasive arterial device will be compared.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

Patients referred to the Non-invasive Vascular Laboratory that have arterial studies to assess for atherosclerosis.

Exclusion Criteria:

Patients unable to have non-invasive vascular arterial studies to assess for atherosclerosis.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location	Status
Rochester, Minn. Mayo Clinic principal investigator Thom Rooke, M.D.	Closed for enrollment

Mayo Clinic Location

Status

Rochester, Minn.

Mayo Clinic principal investigator

Thom Rooke, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Clinical Trials