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Extrait
The objective of this study is to compare the efficacy and safety of two modes of vardenafil therapy versus placebo to treat erectile dysfunction, starting within 14 days following bilateral nerve-sparing radical retropubic prostatectomy (BNSRRP). Specifically, the primary objective is to determine whether early, NIGHTLY dosing with vardenafil significantly improves recovery of erectile function after surgery as compared to placebo, and whether early PRN dosing with vardenafil also improves recovery of function as compared to placebo
Critère d'inclusion
- Erectile Dysfunction