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Completed Phase 4 Interventional Results available

Assessment Of Dutasteride (AVODART) In Extending The Time To Progression Of Low-Risk, Localized Prostate Cancer In Men

ClinicalTrials.gov ID: NCT00363311

Public ClinicalTrials.gov record NCT00363311. 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 17, 2026, 4:29 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 Randomized, Double-Blind, Placebo-Controlled Trial Assessing the Efficacy and Safety of Dutasteride in Extending the Time to Progression of Low-Risk, Localized Prostate Cancer in Men Who Are Candidates for or Undergoing Expectant Management

Brief summary

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

The purpose of this study is to examine the effect of dutasteride on the inhibition of low-risk, localized prostate cancer progression in men who would otherwise receive no active therapy (expectant management).

Study identification

NCT ID
NCT00363311
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
302 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
50 Years to 80 Years
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
Jul 2006 (Type not available)
Primary completion
Mar 2010 (Actual)
Completion
Jul 2010 (Actual)
Last update posted
Jan 18, 2017

2006 – 2010

United States locations

U.S. sites
58
U.S. states
30
U.S. cities
57
Facility City State ZIP Site status
GSK Investigational Site Little Rock Arkansas 72211 —
GSK Investigational Site Beverly Hills California 90210 —
GSK Investigational Site Laguna Hills California 92653 —
GSK Investigational Site Mission Hills California 91345 —
GSK Investigational Site Modesto California 95350 —
GSK Investigational Site San Bernardino California 92404 —
GSK Investigational Site Torrance California 90506 —
GSK Investigational Site Englewood Colorado 80113 —
GSK Investigational Site Wheat Ridge Colorado 80033 —
GSK Investigational Site New Britain Connecticut 06052 —
GSK Investigational Site Trumbull Connecticut 06611 —
GSK Investigational Site Washington D.C. District of Columbia 20307 —
GSK Investigational Site Jacksonville Florida 32224 —
GSK Investigational Site Largo Florida 33773 —
GSK Investigational Site Orlando Florida 32803 —
GSK Investigational Site Roswell Georgia 30076 —
GSK Investigational Site Coeur d'Alene Idaho 83814 —
GSK Investigational Site Chicago Illinois 60612 —
GSK Investigational Site Melrose Park Illinois 60160 —
GSK Investigational Site Fort Wayne Indiana 46825 —
GSK Investigational Site Newburgh Indiana 47630 —
GSK Investigational Site Overland Park Kansas 66211 —
GSK Investigational Site Shreveport Louisiana 71106 —
GSK Investigational Site Annapolis Maryland 21401 —
GSK Investigational Site Greenbelt Maryland 20770 —
GSK Investigational Site Watertown Massachusetts 02472 —
GSK Investigational Site Minneapolis Minnesota — —
GSK Investigational Site Saint Cloud Minnesota 56303 —
GSK Investigational Site Jackson Mississippi 39202 —
GSK Investigational Site St Louis Missouri 63136 —
GSK Investigational Site Las Vegas Nevada 89148 —
GSK Investigational Site Marlton New Jersey 08053 —
GSK Investigational Site Albuquerque New Mexico 87109 —
GSK Investigational Site Albany New York 12208 —
GSK Investigational Site Elmont New York 11003 —
GSK Investigational Site Garden City New York 11530 —
GSK Investigational Site New York New York 10016 —
GSK Investigational Site Orchard Park New York 14127 —
GSK Investigational Site Syracuse New York 13210 —
GSK Investigational Site Greensboro North Carolina 27403 —
GSK Investigational Site Salisbury North Carolina 28144 —
GSK Investigational Site Winston-Salem North Carolina 27103 —
GSK Investigational Site Columbus Ohio 43214 —
GSK Investigational Site Springfield Oregon 97477 —
GSK Investigational Site Bala-Cynwyd Pennsylvania 19004 —
GSK Investigational Site Lancaster Pennsylvania 17604 —
GSK Investigational Site Philadelphia Pennsylvania 19107 —
GSK Investigational Site Memphis Tennessee 38119 —
GSK Investigational Site Nashville Tennessee 37232 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Temple Texas 76508 —
GSK Investigational Site Salt Lake City Utah 84107 —
GSK Investigational Site Richmond Virginia 23235 —
GSK Investigational Site Virginia Beach Virginia 23455 —
GSK Investigational Site Williamsburg Virginia 23185 —
GSK Investigational Site Seattle Washington 98101 —
GSK Investigational Site Seattle Washington 98166 —
GSK Investigational Site Spokane Washington 99202 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00363311, 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 Jan 18, 2017 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00363311 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →