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Evaluation of the Efficacy and Safety of Silodosin in the Treatment of the Signs and Symptoms of BPH

Primary Purpose

Benign Prostatic Hyperplasia

Status
Completed
Phase
Phase 3
Locations
United Kingdom
Study Type
Interventional
Intervention
Silodosin
Tamsulosin
Placebo
Sponsored by
RECORDATI GROUP
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Benign Prostatic Hyperplasia focused on measuring Benign prostatic hyperplasia, alpha-blockers

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

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 Use of concomitant drugs that would confound the efficacy evaluation Use of concomitant drugs that would be unsafe with this alpha-blocker

Sites / Locations

  • Sheffield Teaching Hospitals NHS Foundation Trust, Royal Hallamshire Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

Silodosin

Tamsulosin

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Change in baseline total score on the International Prostate Symptom Score

Secondary Outcome Measures

Change in baseline obstructive subscore of the International Prostate Symptom Score;
change in baseline irritative subscore of the International Prostate Symptom Score;
change in baseline maximum urine flow rate;
safety

Full Information

First Posted
August 2, 2006
Last Updated
February 18, 2009
Sponsor
RECORDATI GROUP
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1. Study Identification

Unique Protocol Identification Number
NCT00359905
Brief Title
Evaluation of the Efficacy and Safety of Silodosin in the Treatment of the Signs and Symptoms of BPH
Official Title
Evaluation of the Efficacy and Safety of Silodosin vs. Tamsulosin and Placebo in the Treatment of the Signs and Symptoms of BPH. Multicentre, Randomised, Double-Blind, Controlled Trial With an Optional Long-Term, Open-Label Extension Phase.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2009
Overall Recruitment Status
Completed
Study Start Date
May 2006 (undefined)
Primary Completion Date
May 2007 (Actual)
Study Completion Date
January 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
RECORDATI GROUP

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
A new drug for the treatment of benign prostatic hyperplasia is compared with placebo and tamsulosin (a drug belonging to the same therapeutic class) for to determine if it is safe and effective (the first phase of the study lasts approximately 18 weeks) and then is used for another 9 months to determine its long-term safety.
Detailed Description
This is a multi-centre, double-blind, placebo and active controlled, parallel 12 week treatment trial in men with signs and symptoms of benign prostatic hyperplasia, followed by a 9 month open-label phase. The following procedures are used: physical exams, electrocardiograms, clinical laboratory tests, vital signs, the International Prostate Symptom Score, maximum urine flow rate, adverse events, concomitant medications, quality of life and compliance. 93 centres in 11 European countries (Finland, France, Germany, Italy, Netherlands, Poland, Romania, Russia, Spain, Ukraine, UK) will be involved

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Benign Prostatic Hyperplasia
Keywords
Benign prostatic hyperplasia, alpha-blockers

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1228 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Silodosin
Arm Type
Experimental
Arm Title
Tamsulosin
Arm Type
Active Comparator
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Silodosin
Other Intervention Name(s)
KMD3213
Intervention Description
8 mg daily for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Tamsulosin
Other Intervention Name(s)
Omnic
Intervention Description
0.4 mg daily for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
once daily for 12 weeks
Primary Outcome Measure Information:
Title
Change in baseline total score on the International Prostate Symptom Score
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Change in baseline obstructive subscore of the International Prostate Symptom Score;
Time Frame
12 weeks
Title
change in baseline irritative subscore of the International Prostate Symptom Score;
Time Frame
12 weeks
Title
change in baseline maximum urine flow rate;
Time Frame
12 weeks
Title
safety
Time Frame
52 weeks

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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 Use of concomitant drugs that would confound the efficacy evaluation Use of concomitant drugs that would be unsafe with this alpha-blocker
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christopher Re Chapple, BSc MD
Organizational Affiliation
Sheffield Teaching Hospitals NHS Foundation Trust, Royal Hallamshire Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sheffield Teaching Hospitals NHS Foundation Trust, Royal Hallamshire Hospital
City
Sheffield
ZIP/Postal Code
S10 2JF
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
25712312
Citation
Osman NI, Chapple CR, Tammela TL, Eisenhardt A, Oelke M. Open-label, 9-month extension study investigating the uro-selective alpha-blocker silodosin in men with LUTS associated with BPH. World J Urol. 2015 May;33(5):697-706. doi: 10.1007/s00345-015-1519-2. Epub 2015 Feb 25.
Results Reference
derived
PubMed Identifier
21109344
Citation
Chapple CR, Montorsi F, Tammela TL, Wirth M, Koldewijn E, Fernandez Fernandez E; European Silodosin Study Group. Silodosin therapy for lower urinary tract symptoms in men with suspected benign prostatic hyperplasia: results of an international, randomized, double-blind, placebo- and active-controlled clinical trial performed in Europe. Eur Urol. 2011 Mar;59(3):342-52. doi: 10.1016/j.eururo.2010.10.046. Epub 2010 Nov 10.
Results Reference
derived

Learn more about this trial

Evaluation of the Efficacy and Safety of Silodosin in the Treatment of the Signs and Symptoms of BPH

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