The purpose of this study is to determine whether Tamuslosin is effective in the treatment of lower urinary tract syndrome with female patients...
Date First Received: September 13, 2005
Last Updated: October 18, 2007
Verified by: Astellas Pharma Inc, October 2007
Clinical Trial Phase: Phase 3 | Start Date:
Overall Status: Completed
Brief Summary
Condition Keyword(s):
Intervention(s):
The purpose of this study is to determine whether Tamuslosin is effective in the treatment of lower urinary tract syndrome with female patients.
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Intervention(s) in this Clinical Trial
- Drug: Tamuslosin
Criteria for Participation in this Clinical Trial
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.
Gender Eligibility for this Clinical Trial: Female
Minimum Age for this Clinical Trial: 20 Years
Maximum Age for this Clinical Trial: 90 Years
Are Healthy Volunteers Accepted for this Clinical Trial?: No
Clinical Trial Sponsor Information
Lead Sponsor: Astellas Pharma Inc
Overall Clinical Trial Officials and Contacts
Study Director Study Chair Clinical Development, Astellas Pharma Inc.
Additional Information
Information obtained from ClinicalTrials.gov on November 19, 2008
Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00239265
Study ID Number: B6171/LCT2
ClinicalTrials.gov Identifier: NCT00239265
Health Authority: Japan: Ministry of Health, Labor and Welfare
Clinical Trials Authorship and Review
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