Vardenafil Improves Erectile Function in Men with Erectile Dysfunction Irrespective of Disease Severity and Disease Classification

• Published in: Journal of sexual medicine 2004-11, Vol.1 (3), p.301-309
• Main Authors: Donatucci, Craig, Eardley, Ian, Buvat, Jacques, Gittelman, Marc, Kell, Phillip, Segerson, Thom, Homering, Martin, Montorsi, Francesco
• Format: Article
• Language: English
• Subjects: 3',5'-Cyclic-GMP Phosphodiesterases; Cyclic Nucleotide Phosphodiesterases, Type 5; Disease Classification; Double-Blind Method; Drug Administration Schedule; Erectile Dysfunction; Erectile Dysfunction - classification; Erectile Dysfunction - drug therapy; Erectile Dysfunction - physiopathology; Humans; Imidazoles - administration & dosage; Imidazoles - therapeutic use; Male; Middle Aged; Penile Erection - drug effects; Phosphodiesterase Inhibitors - administration & dosage; Phosphodiesterase Inhibitors - therapeutic use; Phosphoric Diester Hydrolases - metabolism; Piperazines - administration & dosage; Piperazines - therapeutic use; Retrospective Studies; Severity of Illness Index; Sulfones - administration & dosage; Sulfones - therapeutic use; Triazines - administration & dosage; Triazines - therapeutic use; Vardenafil; Vardenafil Dihydrochloride
• ISSN: 1743-6095; 1743-6109
• DOI: 10.1111/j.1743-6109.04043.x

Vardenafil (Levitra®) is a potent and selective phosphodiesterase 5 (PDE5) inhibitor used in the management of erectile dysfunction (ED). This retrospective subgroup analysis assessed the effectiveness of vardenafil treatment in men with ED of different baseline severity and disease classification. Data from two pivotal, randomized, double‐blind, placebo‐controlled clinical trials enrolling men from the general ED population who received placebo or vardenafil 5 mg, 10 mg, or 20 mg during a 12‐week treatment period were retrospectively analysed, stratifying by psychogenic, organic, and mixed ED disease classification as determined by the investigator. Efficacy endpoints included the International Index of Erectile Function (IIEF)‐Erectile Function (EF) domain score, per‐patient diary response rates to questions on penile insertion [Sexual Encounter Profile (SEP‐2)] and maintenance of erection (SEP‐3) and rates of positive response to the Global Assessment Question (GAQ). Data from 1,385 men who received at least one dose of study medication and had pre‐ and post‐baseline measures of efficacy available (intent‐to‐treat population) are presented. At baseline 37–41% of patients had severe ED, 30–34% moderate, 22% mild‐to‐moderate and 6–8% mild ED. At baseline, 46–51% of patients were considered to have an organic cause for ED, 13–16% psychogenic ED, and 36–38% mixed classification of ED. For all classifications and for mild‐to‐moderate to severe ED, men treated with 10 or 20 mg of vardenafil showed statistically and clinically  significant  improvements  (P