| Protocol ID: |
101722 |
| Clinical Study ID: |
101722 |
| Official Title: |
Prospective, national, multicentre, non comparative study evaluating the improvement of urinary symptoms, discomfort and quality of life in subjects with benign prostatic hyperplasia (BPH) after 24 weeks of treatment by dutasteride. |
| Phase: |
Phase 4 |
| Study Indications or Diseases: |
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| Generic Name: |
dutasteride |
| Trade/Product Name: |
Duagen,Zytefor,Avolve,Avodart,Avidart,Zyfetor |
| Approved Drug Label: |
http://www.gsk.com/products/prescription-medicines/index.htm |
| Results Summary: |
Click here to download result summary.
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| Citations: |
- Desgrandchamps F, Droupy S, Irani J, Saussine C, Comenducci A. Effect of dutasteride on the symptoms of benign prostatic hyperplasia, and patient quality of life and discomfort, in clinical practice. BJU International 2006; 98(1): 83-88
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