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Completed Phase 2 Interventional Results available

Study of Silodosin to Facilitate Passage of Urinary Stones

ClinicalTrials.gov ID: NCT01144949

Public ClinicalTrials.gov record NCT01144949. 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, 1:05 AM 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 Study of Silodosin to Facilitate Urinary Stone Passage

Brief summary

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

The purpose of this study is to assess if patients treated with silodosin will have a higher spontaneous passage rate of their ureteral stone than those treated with placebo.

Study identification

NCT ID
NCT01144949
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Watson Pharmaceuticals
Industry
Enrollment
239 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Jun 2010 (Type not available)
Primary completion
Jul 2012 (Actual)
Completion
Jul 2012 (Actual)
Last update posted
Aug 11, 2014

2010 – 2012

United States locations

U.S. sites
27
U.S. states
13
U.S. cities
27
Facility City State ZIP Site status
Watson Investigational Site Birmingham Alabama — —
Watson Investigational Site Anchorage Alaska — —
Watson Investigative Site Mission Hills California — —
Watson Investigational Site Murrieta California — —
Watson Investigational Site San Diego California — —
Watson Investigational Site Daytona Beach Florida — —
Watson Investigational Site Gainesville Florida — —
Watson Investigational Site Orange City Florida — —
Watson Investigative Site Overland Park Kansas — —
Watson Investigative Site North Kansas City Missouri — —
Watson Investigational Site Hackensack New Jersey — —
Watson Investigational Site Mount Laurel New Jersey — —
Watson Investigational Site Sewell New Jersey — —
Watson Investigational Site Voorhees Township New Jersey — —
Watson Investigational Site Albany New York — —
Watson Investigational Site Garden City New York — —
Watson Investigational Site New York New York — —
Watson Investigational Site Plainview New York — —
Watson Investigational Site Syracuse New York — —
Watson Investigational Site Cincinnati Ohio — —
Watson Investigational Site Columbus Ohio — —
Watson Investigational Site Bala-Cynwyd Pennsylvania — —
Watson Investigational Site Lancaster Pennsylvania — —
Watson Investigational Site Myrtle Beach South Carolina — —
Watson Investigational Site Dallas Texas — —
Watson Investigational Site San Antonio Texas — —
Watson Investigational Site Virginia Beach Virginia — —

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 NCT01144949, 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 Aug 11, 2014 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01144949 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →