Primary Objective: * To assess the sexual function of Benign Prostatic Hyperplasia patients Secondary Objective: * To evaluate the association between Lower Urinary Tract Symptoms severity and sexual disorders * To compare the sexual function, urinary symptoms and Quality of Life of Benign Prostatic Hyperplasia patients on XATRAL 10mg OD among the different regions * To correlate the Male Sexual Health Questionnaire(MSHQ) and 5-item version of the International Index of Erectile Function (IIEF-5) * To assess the onset of action of XATRAL 10mg OD * To assess the peak urinary flow rate * To assess the safety and the tolerability of XATRAL 10mg OD
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
362
One tablet of XATRAL® 10mg OD once a day at the end of an evening meal. The tablets had to be swallowed whole without being chewed or crushed
Sanofi-Aventis Administrative Office
Taipei, Taiwan
Male Sexual Health Questionnaire Ejaculation score (MSHQ)
Time frame: At week 24
MSHQ Ejaculation score
Time frame: At week 14, 12 and 24
International Prostate Symptom Score (I-PSS) including quality of life index
Time frame: At week 1, 4, 12 and 24
Systolic and diastolic blood pressure
Time frame: At week 1, 4, 12 and 24
Heart rate
Time frame: At week 1, 4, 12 and 24
Prostate Specific Antigen
Time frame: At week 24
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