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| Sponsor: | Astellas Pharma Inc |
|---|---|
| Information provided by: | Astellas Pharma Inc |
| ClinicalTrials.gov Identifier: | NCT00239317 |
Purpose
The purpose of this study is to determine whether Tamusulosin is effective in the treatment of lower urinary tract syndrome with male patients.
| Condition | Intervention | Phase |
|---|---|---|
|
Urinary Tract Diseases |
Drug: Tamusulosin |
Phase III |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double-Blind Primary Purpose: Treatment |
Eligibility| Ages Eligible for Study: | 20 Years to 90 Years |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Japan | |
| Chubu region, Japan | |
| Chugoku region, Japan | |
| Hokkaido region, Japan | |
| Kanto region, Japan | |
| Kinki region, Japan | |
| Kyushu region, Japan | |
| Touhoku region, Japan | |
| Study Director: | Study Director | Clinical Development, Astellas Pharma Inc. |
More Information
| ClinicalTrials.gov Identifier: | NCT00239317 History of Changes |
| Other Study ID Numbers: | B617/LCT3 |
| Study First Received: | September 19, 2005 |
| Last Updated: | October 18, 2007 |
| Health Authority: | Japan: Ministry of Health, Labor and Welfare |
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tamsulosin urinary tract diseases male |
|
Urologic Diseases Tamsulosin Adrenergic alpha-1 Receptor Antagonists Adrenergic alpha-Antagonists Adrenergic Antagonists |
Adrenergic Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Physiological Effects of Drugs |