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Completed Phase 2 Interventional Results available

A Study of Silodosin 8 mg Daily for the Treatment of Nocturia in Men With Benign Prostatic Hyperplasia

ClinicalTrials.gov ID: NCT00793819

Public ClinicalTrials.gov record NCT00793819. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 12:02 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Double-Blind, Placebo-Controlled Phase 2 Study of Silodosin 8 mg Daily for the Treatment of Nocturia in Men With Benign Prostatic Hyperplasia

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Silodosin is compared to placebo to determine if it is safe and effective for the treatment of nighttime urination (nocturia) in men with BPH

Study identification

NCT ID
NCT00793819
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Watson Pharmaceuticals
Industry
Enrollment
215 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
50 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 2009 (Type not available)
Primary completion
Oct 2009 (Actual)
Completion
Oct 2009 (Actual)
Last update posted
Mar 9, 2012

2009

United States locations

U.S. sites
27
U.S. states
20
U.S. cities
27
Facility City State ZIP Site status
Watson Investigational Site Huntsville Alabama — —
Watson Investigational Site Laguna Hills California — —
Watson Investigational Site San Diego California — —
Watson Investigational Site Aventura Florida — —
Watson Investigational Site Clearwater Florida — —
Watson Investigational Site Orlando Florida — —
Watson Investigational Site Marietta Georgia — —
Watson Investigational Site Sandy Springs Georgia — —
Watson Investigational Site Coeur d'Alene Idaho — —
Watson Investigational Site West Des Moines Iowa — —
Watson Investigational Site Paducah Kentucky — —
Watson Investigational Site Greenbelt Maryland — —
Watson Investigational Site Troy Michigan — —
Watson Investigational Site Missoula Montana — —
Watson Investigational Site Omaha Nebraska — —
Watson Investigational Site Las Vegas Nevada — —
Watson Investigational Site Lawrenceville New Jersey — —
Watson Investigational Site Albuquerque New Mexico — —
Watson Investigational Site Bay Shore New York — —
Watson Investigational Site New York New York — —
Watson Investigational Site Williamsville New York — —
Watson Investigational Site Concord North Carolina — —
Watson Investigational Site Salisbury North Carolina — —
Watson Investigational Site Bethany Oklahoma — —
Watson Investigational Site Bala-Cynwyd Pennsylvania — —
Watson Investigational Site Myrtle Beach South Carolina — —
Watson Investigational Site Burien Washington — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00793819, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 9, 2012 · Synced Oct 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00793819 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →