A Study to Define Success After Artificial Urinary Sphincter Placement in Men from Patient Subjective and Objective Assessment

Overview

About this study

The purpose of this study is to define the successful placement of the Artificial Urinary Sphincter in Men, by collecting and comparing patient subjective and objective assessment data. 

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

  • Undergoing AUS placement in the management of male stress urinary incontinence from 1983-2016

Exclusion Criteria

  • Female and/or younger than 18 years old

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

Daniel Elliott, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available

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CLS-20272720

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