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RESTORE Study

A Prospective Randomized Control Trial to Compare the Efficacy of the Revi System Therapy on Versus off in Relieving Urinary Urge Incontinence Episodes

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AGE: 18+ years old
TYPE: Interventional Study
CONDITION: Overactive Bladder (OAB)
LOCATIONS: University Hospitals Ahuja Medical Center, University Hospitals Beachwood Medical Center, University Hospitals Geauga Medical Center, University Hospitals Portage Medical Center, University Hospitals St. Johns Medical Center

Learn More About This Research Study

For more information, please contact the study team at 216-844-8092 or complete the form below.

Purpose of the Study

The purpose of this research study is to evaluate the effectiveness of the Revi System therapy in the treatment of urinary urge incontinence. Revi is a small FDA-approved device implanted near the ankle that stimulates the tibial nerve, which can help calm the bladder.

Who Can Participate

Individuals who suffer from symptoms of urgency incontinence alone or in combination with urinary urgency and are 18 years of age or older may meet the requirements for participation in this study.

Request More Information

If you would like to be contacted by a study team member for more information about this study, please provide your contact information below.

Requestor's Information

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  • STUDY ID# 20231566