Clinical Trials Directory

Trials / Completed

CompletedNCT00941343

Benign Prostatic Hyperplasia in Taiwan

Sexuality and Management of Benign Prostatic Hyperplasia With Alfuzosin

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
362 (actual)
Sponsor
Sanofi · Industry
Sex
Male
Age
40 Years
Healthy volunteers
Not accepted

Summary

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

Conditions

Interventions

TypeNameDescription
DRUGAlfuzosin (XATRAL® - SL770499)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

Timeline

Start date
2006-09-01
Primary completion
2008-09-01
Completion
2008-09-01
First posted
2009-07-17
Last updated
2010-03-30

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT00941343. Inclusion in this directory is not an endorsement.