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Completed Phase 3 Interventional Results available

A New Drug for Benign Prostatic Hyperplasia (BPH) Compared With Placebo

ClinicalTrials.gov ID: NCT00224107

Public ClinicalTrials.gov record NCT00224107. 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 Jul 22, 2026, 5:10 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 Multi-Center, Randomized, Double-Blind, Placebo Controlled, Parallel Evaluation of the Efficacy and Safety of a New Drug in the Treatment of the Signs and Symptoms of Benign Prostatic Hyperplasia

Study identification

NCT ID
NCT00224107
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Watson Pharmaceuticals
Industry
Enrollment
461 participants

Conditions and interventions

Interventions

  • Silodosin Drug
  • Placebo Other

Drug · Other

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
Apr 30, 2005
Primary completion
Jul 31, 2006
Completion
Jul 31, 2006
Last update posted
Jul 11, 2011

2005 – 2006

United States locations

U.S. sites
43
U.S. states
24
U.S. cities
43
Facility City State ZIP Site status
Not listed Huntsville Alabama
Not listed Tucson Arizona
Not listed Anaheim California
Not listed Culver City California
Not listed Irvine California
Not listed La Jolla California
Not listed Long Beach California
Not listed Newport Beach California
Not listed San Diego California
Not listed Aurora Colorado
Not listed Wheat Ridge Colorado
Not listed Waterbury Connecticut
Not listed Aventura Florida
Not listed Clearwater Florida
Not listed Coral Gables Florida
Not listed Pensacola Florida
Not listed Marietta Georgia
Not listed Chicago Illinois
Not listed Peoria Illinois
Not listed Des Moines Iowa
Not listed Saint Joseph Michigan
Not listed Edina Minnesota
Not listed Missoula Montana
Not listed Las Vegas Nevada
Not listed Bay Shore New York
Not listed Garden City New York
Not listed Manhasset New York
Not listed New York New York
Not listed Staten Island New York
Not listed Williamsville New York
Not listed Charlotte North Carolina
Not listed Salisbury North Carolina
Not listed Winston-Salem North Carolina
Not listed Cincinnati Ohio
Not listed Bethany Oklahoma
Not listed Portland Oregon
Not listed Lancaster Pennsylvania
Not listed Greer South Carolina
Not listed Dallas Texas
Not listed Salt Lake City Utah
Not listed Lakewood Washington
Not listed Tacoma Washington
Not listed Milwaukee Wisconsin

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 NCT00224107, 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 Jul 11, 2011 · Synced Jul 22, 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 protocol, eligibility criteria, and contact information for NCT00224107 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →