Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

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

Study information

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

Clinical Trial Summary

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


Recruitment information / eligibility

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.

Study Design

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


Related Conditions & MeSH terms


Intervention

Drug:
Tamuslosin


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Astellas Pharma Inc

Country where clinical trial is conducted

Japan, 

See also
  Status Clinical Trial Phase
Completed NCT02805504 - Liposomal Bupivacaine for Postoperative Pain Control in Urologic Procedures Phase 4
Completed NCT00239317 - Tamsulosin Phase III Clinical Trial -Double-Blind, Placebo Controlled Study in Male Patients With Lower Urinary Tract Syndrome Phase 3