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A Study to Gather Information on the Effectiveness of the Phillips Lumify Portable Ultrasound Device in Detecting the Posterior Tibial Nerve

Overview

About this study

The purpose of this study is to determine efficacy of the Philips Lumify ultrasound in detecting the posterior tibial nerve.

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:

  • Female only, ages 18 or older

Exclusion Criteria:

  • In order to determine the actual efficacy of the Philips Lumify Ultrasound exam, we will be approaching all patients, independent of their medical history.

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

Jacksonville, Fla.

Mayo Clinic principal investigator

Steven Petrou, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

More about research at Mayo Clinic

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CLS-20428802

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