The purpose of this study is to determine whether tamsulosin and tolterodine are effective in
the treatment of men with lower urinary tract symptoms and chronic prostatitis/chronic pelvic
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Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT00913315
Ages eligible for Study
18 Years to 45 Years
Genders eligible for Study
Accepts Healthy Volunteers
diagnosis of CP/CPPS based on the classification of US National Institutes of Health, aged 18-45 years
total score of at least 12 on the National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI)
urinary score of at least 4 on the CPSI
subjects who anticipate improving symptoms
previous treatment with any other alpha-adrenergic receptor blocker and antimuscarinic agents for symptoms of CP/CPPS or for any other reason
those who had had previous urinary tract infection with the last year
those who had been treat or were taking medication that could affect lower urinary tract function
those who met the criteria for chronic bacterial prostatitis after lower urinary tract localization studies
those who had other significant medical problems
All locations for NCT00913315
Department of Urology, the First Affiliated Hospital of Chongqing Medical University
Chongqing, Chongqing, China, 400016
not yet recruiting
View full eligibility
Tris trial is registered with FDA with number: NCT00913315. The sponsor of the trial is Chongqing Medical University and it is looking for 30 volunteers for the current phase.
Official trial title: Efficacy Study of Tamsulosin and Tolterodine Treatment of Men With Chronic Prostatitis/Chronic Pelvic Pain Syndrome and Lower Urinary Tract Symptoms
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