An Implantable Microstimulator for the Chronic Treatment of Urinary Urgency-Frequency Syndrome

Completed · Phase 3

Conditions studied: Overactive Bladder

In brief

The goal of this study is to investigate the safety and effectiveness of a new implanted device designed to treat Urinary Urgency-Frequency Syndrome.

Key facts

Study ID

NCT00131573

Run by

Boston Scientific Corporation

People needed

118

Starts

2004-05-01

Expected to finish

2012-12-01

Last updated by the study team

2013-11-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

• Arizona Health Sciences Center — Tucson, Arizona, United States
• The Department of Urology, Stanford University Medical Center — Stanford, California, United States
• Milestone Medical Research — Englewood, Colorado, United States
• Walter Reed Army Medical Center — Washington D.C., District of Columbia, United States
• Overland Park Regional Medical Center — Overland Park, Kansas, United States
• William Beaumont Hospital — Royal Oak, Michigan, United States
• Cornerstone Medical Specialty Center — Woodbury, Minnesota, United States
• New York University — New York, New York, United States
• Cleveland Clinic Foundation — Cleveland, Ohio, United States
• The Pelvic and Sexual Health Institute — Philadelphia, Pennsylvania, United States
• Dallas Center for Pelvic Medicine — Dallas, Texas, United States

Full record on ClinicalTrials.gov

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