Clinical Trial to Compare the Efficacy and Safety of Solifenacin/Tamsulosin Combination Therapy with Tamsulosin Monotherapy for Lower Urinary Tract Symptoms due to Benign Prostatic Hyperplasia
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
780
Tamsulosin 0.2mg + Solifenacin 5mg for 12wks
Tamsulosin 0.2mg + Placebo(Solifenacin) for 12wks
Asan Medical Center
Seoul, South Korea
change of TUFS
Time frame: 12 weeks from baseline
change of total IPSS
Time frame: 12 weeks from baseline
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