Trial Information

Summary: Study for Female Patients with Overactive Bladders and Urge Urinary Incontinence

Description: Do you find yourself needing to run to the bathroom all the time. Always feeling like you have to use the facilities? This is a short term, four visit, phase II clinical research study to evaluate the dose response characteristics of an approved medication.

We need study volunteers for this short term dose range finding study.

Visit one is a screening visit. A 14 day screening period follows visit one. Visit two includes a single-blind placebo dosing. A two day treatment period follows - Visits three and four require a 4-5 hour stay at the clinic.

To Qualify: Have a diagnosis of Overactive Bladder or Urge Incontinence. You must have at least nine urine voids per day (in a 24 hour period) over a 14 day observation period. You must encounter or have at least two episodes of urge incontinence during this 14 day period. Additional qualifications include: Women who are between the ages of 18-70 years of age, in good general health, without high blood pressure, not pregnant, willing to use medically acceptable contraception (or surgically sterile), sign Consent for the study, and be able to attend all study visits. Other parameters apply.

Compensation: Qualified participants may receive: study related medical exams (physical exam) and blood test analyses, bladder ultrasound and compensation for time and travel.

Location: The study is being conducted at the Salt Lake Women’s Center, which is located in Sandy, UT. Click on the more information button below.

**Note: Participants need to live within the intermountain region.

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Trial listings updated: June 1, 2008 at 5:43:23 AM