Urinary Tract Diseases Clinical Trial
NCT number | NCT00239265 |
Other study ID # | B6171/LCT2 |
Secondary ID | |
Status | Completed |
Phase | Phase 3 |
First received | September 13, 2005 |
Last updated | October 18, 2007 |
Verified date | October 2007 |
Source | Astellas Pharma Inc |
Contact | n/a |
Is FDA regulated | No |
Health authority | Japan: Ministry of Health, Labor and Welfare |
Study type | Interventional |
The purpose of this study is to determine whether Tamuslosin is effective in the treatment of lower urinary tract syndrome with female patients.
Status | Completed |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 20 Years to 90 Years |
Eligibility |
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. |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Astellas Pharma Inc |
Japan,
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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