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Therapeutic Areas: Nephrology | Obstetrics/Gynecology (Women’s Health) | Urology | Family Medicine
Disease Category: Urinary Incontinence
Location: United States, IN
Study to confirm the efficacy of Fesoterodine 4 mg compared to 8 mg.
The purpose of this study is to compare the effectiveness of two doses of a drug called Fesoterodine and placebo (a substance that contains no active ingredient but looks identical to the study drug) for overactive bladder. In order to achieve this evaluation in an unbiased manner, you will be randomly assigned to one of 3 groups: Fesoterodine 4 mg, Fesoterodine 8 mg, or Placebo.
Patient Inclusion Criteria:
Patient Exclusion Criteria:
Date Last Changed:
May 2, 2014
Kristen Willinger, Research RecruiterFirst Urology, PSC101 Hospital BlvdJeffersonville, IN 47130Phone: (812) 206-8166Fax: (812) 288-2612
Research Center Information: First Urology, PSC
If you would like to learn more about participating in this research study, please email the trial contact using the form below.
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