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
| Type | Name | Description |
|---|---|---|
| DRUG | Alfuzosin (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.