- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00224107
A New Drug for Benign Prostatic Hyperplasia (BPH) Compared With Placebo
July 5, 2011 updated by: Watson Pharmaceuticals
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
A new drug for benign prostatic hyperplasia is compared to placebo for to determine if it is safe and effective.
The study lasts approximately 20 weeks.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This will be a multi-center, double-blind, placebo controlled, parallel, 12 week treatment trial in men with signs and symptoms of benign prostatic hyperplasia.
The following procedures are utilized: physical exams, electrocardiograms, clinical laboratory tests, vital signs, the International Prostate Symptom Score, maximum urine flow rate, pharmacokinetics, adverse events, concomitant medications, quality of life, and compliance.
Study Type
Interventional
Enrollment (Actual)
461
Phase
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Alabama
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Huntsville, Alabama, United States
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Arizona
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Tucson, Arizona, United States
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California
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Anaheim, California, United States
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Culver City, California, United States
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Irvine, California, United States
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La Jolla, California, United States
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Long Beach, California, United States
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Newport Beach, California, United States
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San Diego, California, United States
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Colorado
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Aurora, Colorado, United States
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Wheat Ridge, Colorado, United States
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Connecticut
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Waterbury, Connecticut, United States
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Florida
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Aventura, Florida, United States
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Clearwater, Florida, United States
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Coral Gables, Florida, United States
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Pensacola, Florida, United States
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Georgia
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Marietta, Georgia, United States
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Illinois
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Chicago, Illinois, United States
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Peoria, Illinois, United States
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Iowa
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Des Moines, Iowa, United States
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Michigan
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St. Joseph, Michigan, United States
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Minnesota
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Edina, Minnesota, United States
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Montana
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Missoula, Montana, United States
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Nevada
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Las Vegas, Nevada, United States
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New York
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Bay Shore, New York, United States
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Garden City, New York, United States
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Manhasset, New York, United States
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New York, New York, United States
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Staten Island, New York, United States
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Williamsville, New York, United States
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North Carolina
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Charlotte, North Carolina, United States
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Salisbury, North Carolina, United States
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Winston-Salem, North Carolina, United States
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Ohio
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Cincinnati, Ohio, United States
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Oklahoma
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Bethany, Oklahoma, United States
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Oregon
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Portland, Oregon, United States
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Pennsylvania
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Lancaster, Pennsylvania, United States
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South Carolina
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Greer, South Carolina, United States
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Texas
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Dallas, Texas, United States
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Utah
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Salt Lake City, Utah, United States
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Washington
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Lakewood, Washington, United States
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Tacoma, Washington, United States
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Wisconsin
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Milwaukee, Wisconsin, United States
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
50 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Males in good general health and at least 50 years of age, with symptoms of moderate to severe benign prostatic hyperplasia.
Exclusion Criteria:
- Medical conditions that would confound the efficacy evaluation.
- Medical conditions in which it would be unsafe to use an alpha-blocker.
- The use of concomitant drugs that would confound the efficacy evaluation.
- The use of concomitant drugs that would be unsafe with this alpha-blocker.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: Silodosin
Silodosin 8 mg once daily with food
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8 mg daily for 12 weeks
Other Names:
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Placebo Comparator: placebo
Matching Placebo capsule once daily with food
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1 capsule daily for 12 weeks
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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International Prostate Symptom Score (IPSS)
Time Frame: 12 weeks
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Change from baseline In IPSS at Week 12. IPSS uses a 0 to 35 scale; 0 best, 35 worse symptoms
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12 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Maximum Urine Flow Rate (Qmax)
Time Frame: 12 weeks
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Change from baseline in maximum urine flow rate (Qmax)at Week 12
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12 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Lawrence Hill, PharmD, RPh, Watson Pharmaceuticals
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Marks LS, Gittelman MC, Hill LA, Volinn W, Hoel G. Rapid efficacy of the highly selective alpha(1A)-adrenoceptor antagonist silodosin in men with signs and symptoms of benign prostatic hyperplasia: pooled results of 2 phase 3 studies. J Urol. 2013 Jan;189(1 Suppl):S122-8. doi: 10.1016/j.juro.2012.11.020.
- Roehrborn CG, Kaplan SA, Lepor H, Volinn W. Symptomatic and urodynamic responses in patients with reduced or no seminal emission during silodosin treatment for LUTS and BPH. Prostate Cancer Prostatic Dis. 2011 Jun;14(2):143-8. doi: 10.1038/pcan.2010.46. Epub 2010 Dec 7.
- Marks LS, Gittelman MC, Hill LA, Volinn W, Hoel G. Rapid efficacy of the highly selective alpha1A-adrenoceptor antagonist silodosin in men with signs and symptoms of benign prostatic hyperplasia: pooled results of 2 phase 3 studies. J Urol. 2009 Jun;181(6):2634-40. doi: 10.1016/j.juro.2009.02.034. Epub 2009 Apr 16.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2005
Primary Completion (Actual)
August 1, 2006
Study Completion (Actual)
August 1, 2006
Study Registration Dates
First Submitted
September 14, 2005
First Submitted That Met QC Criteria
September 14, 2005
First Posted (Estimate)
September 22, 2005
Study Record Updates
Last Update Posted (Estimate)
July 12, 2011
Last Update Submitted That Met QC Criteria
July 5, 2011
Last Verified
July 1, 2011
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pathologic Processes
- Prostatic Diseases
- Prostatic Hyperplasia
- Hyperplasia
- Physiological Effects of Drugs
- Adrenergic Antagonists
- Adrenergic Agents
- Neurotransmitter Agents
- Molecular Mechanisms of Pharmacological Action
- Urological Agents
- Adrenergic alpha-1 Receptor Antagonists
- Adrenergic alpha-Antagonists
- Silodosin
Other Study ID Numbers
- SI04009
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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