Tamsulosin Phase III Clinical Trial -Double-Blind, Placebo Controlled Study in Female Patients With Lower Urinary Tract Syndrome

This study has been completed.
Information provided by:
Astellas Pharma Inc
ClinicalTrials.gov Identifier:
First received: September 13, 2005
Last updated: October 18, 2007
Last verified: October 2007

The purpose of this study is to determine whether Tamuslosin is effective in the treatment of lower urinary tract syndrome with female patients.

Condition Intervention Phase
Urinary Tract Diseases
Drug: Tamuslosin
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double-Blind
Primary Purpose: Treatment

Further study details as provided by Astellas Pharma Inc:


Ages Eligible for Study:   20 Years to 90 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Patients with urination disorder not accompanied by apparent organic or neurologic abnormality(lower urinary tract syndrome: LUTs).

Exclusion Criteria:

  • Patients with urination disorder accompanied by apparent organic or neurologic abnormality, active urinary tract infections, severe cardiovascular, hepatic and/or kidney complications.
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00239265

Chubu region, Japan
Chugoku region, Japan
Hokkaido region, Japan
Kinki region, Japan
Kyushu region, Japan
Touhoku region, Japan
Sponsors and Collaborators
Astellas Pharma Inc
Study Chair: Study Director Clinical Development, Astellas Pharma Inc.
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00239265     History of Changes
Other Study ID Numbers: B6171/LCT2
Study First Received: September 13, 2005
Last Updated: October 18, 2007
Health Authority: Japan: Ministry of Health, Labor and Welfare

Keywords provided by Astellas Pharma Inc:
urinary tract diseases

Additional relevant MeSH terms:
Urologic Diseases

ClinicalTrials.gov processed this record on March 26, 2015