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| Sponsor: | Astellas Pharma Inc |
|---|---|
| Information provided by: | Astellas Pharma Inc |
| ClinicalTrials.gov Identifier: | NCT00239265 |
Purpose
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 III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study |
Eligibility| Ages Eligible for Study: | 20 Years to 90 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Japan | |
| Hokkaido region, Japan | |
| Touhoku region, Japan | |
| Chubu region, Japan | |
| Kyushu region, Japan | |
| Chugoku region, Japan | |
| Kinki region, Japan | |
| Study Chair: | Study Director | Clinical Development, Astellas Pharma Inc. |
More Information
| Study ID Numbers: | B6171/LCT2 |
| Study First Received: | September 13, 2005 |
| Last Updated: | October 18, 2007 |
| ClinicalTrials.gov Identifier: | NCT00239265 History of Changes |
| Health Authority: | Japan: Ministry of Health, Labor and Welfare |
|
tamsulosin urinary tract diseases female |
|
Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Adrenergic Agents Urologic Diseases Antineoplastic Agents Therapeutic Uses |
Physiological Effects of Drugs Tamsulosin Adrenergic Antagonists Adrenergic alpha-Antagonists Pharmacologic Actions |