Vardenafil, a new phosphodiesterase type 5 inhibitor, in the treatment of Erectile dysfunction in men with diabetes: A multicenter double-blind placebo-controlled fixed-dose study

This study evaluated the efficacy and safety of vardenafil treatment for erectile dysfunction (ED) in men with diabetes. In this prospective multicenter double-blind placebo-controlled fixed-dose parallel-group phase III trial, 452 patients with diabetes (type 1 or type 2) and ED were randomized to...

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Veröffentlicht in:Diabetes care 2003-03, Vol.26 (3), p.777-783
Hauptverfasser: GOLDSTEIN, Irwin, YOUNG, Jay M, FISCHER, Jerome, BANGERTER, Keith, SEGERSON, Thomas, TAYLOR, Terry
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Sprache:eng
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Zusammenfassung:This study evaluated the efficacy and safety of vardenafil treatment for erectile dysfunction (ED) in men with diabetes. In this prospective multicenter double-blind placebo-controlled fixed-dose parallel-group phase III trial, 452 patients with diabetes (type 1 or type 2) and ED were randomized to take 10 or 20 mg vardenafil or placebo as needed for 12 weeks. Efficacy responses were assessed by International Index of Erectile Function domain scores, rates of vaginal penetration and successful intercourse, and a global assessment question (GAQ) about erection improvement during the previous 4 weeks. After 12 weeks of treatment, a dose-dependent (P = 0.02) improvement in erections was noted for the GAQ, with 57 and 72% of men taking 10 mg or 20 mg vardenafil, respectively, reporting improved erections, in contrast to 13% after taking placebo (P < 0.0001). For the erectile function domain, dose-dependent (P = 0.03) final scores for the 10- and 20-mg dose were 17.1 and 19.0 compared with 12.6 for placebo (P < 0.0001). Both vardenafil doses significantly enhanced the rates of successful penetration (P < 0.0001) and successful intercourse (P < 0.0001) compared with placebo. Vardenafil treatment was effective in increasing intercourse success rates at all levels of baseline ED severity, at each level of plasma HbA(1c), and for type 1 and 2 diabetes. Treatment-emergent adverse events were primarily mild to moderate headache (
ISSN:0149-5992
1935-5548
DOI:10.2337/diacare.26.3.777