To collect under daily practice conditions, clinical data on the changes of sexual function when a new formulation of alfuzosin(Xatral XL® )is administered once daily in patients with lower urinary tract symptoms(LUTS) suggestive of prostatic hypertrophy
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
166
Sanofi-Aventis
Seoul, South Korea
IIEF and GEQ (Global Efficacy Question)
Time frame: at intermediate visit (M1) and at end-point visit(M3)
blood pressure and heart rate measure in sitting position
Time frame: at each visit
IPSS and Quality of Life Score
Time frame: at intermediate visit (M1) and at end-point visit(M3)
Maximum flow rate and post voiding residual urine
Time frame: at end-point visit(M3)
Spontaneous reported adverse events
Time frame: During all the study period
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