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Completed Phase 2 Interventional Results available

Use of Silodosin to Treat Moderate to Severe Abacterial Chronic Prostatitis/Chronic Pelvic Pain Syndrome.

ClinicalTrials.gov ID: NCT00740779

Public ClinicalTrials.gov record NCT00740779. 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 21, 2026, 4:33 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, Double-Blind, Placebo-Controlled Investigation of Silodosin in the Treatment of Subjects With Moderate to Severe Abacterial Chronic Prostatitis/Chronic Pelvic Pain Syndrome

Study identification

NCT ID
NCT00740779
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Watson Pharmaceuticals
Industry
Enrollment
153 participants

Conditions and interventions

Interventions

  • Silodosin 8 mg Drug
  • Placebo Drug
  • Silodosin 4 mg Drug

Drug

Eligibility (public fields only)

Age range
18 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
Aug 31, 2008
Primary completion
Sep 30, 2009
Completion
Sep 30, 2009
Last update posted
Feb 23, 2012

2008 – 2009

United States locations

U.S. sites
22
U.S. states
15
U.S. cities
22
Facility City State ZIP Site status
Watson Investigational Site San Diego California
Watson Investigational Site Denver Colorado
Watson Investigational Site Columbus Georgia
Watson Investigational Site Roswell Georgia
Watson Investigational Site Jeffersonville Indiana
Watson Investigational Site West Des Moines Iowa
Watson Investigational Site Baltimore Maryland
Watson Investigational Site Boston Massachusetts
Watson Investigational Site Watertown Massachusetts
Watson Investigational Site Omaha Nebraska
Watson Investigational Site Voorhees Township New Jersey
Watson Investigational Site Albuquerque New Mexico
Watson Investigational Site Garden City New York
Watson Investigational Site Kingston New York
Watson Investigational Site New York New York
Watson Investigational Site Poughkeepsie New York
Watson Investigational Site Columbus Ohio
Watson Investigational Site Bethany Oklahoma
Watson Investigational Site Edmond Oklahoma
Watson Investigational Site State College Pennsylvania
Watson Investigational Site Mountlake Terrace Washington
Watson Investigational Site Spokane 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 NCT00740779, 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 Feb 23, 2012 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00740779 live on ClinicalTrials.gov.

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