A Randomised, Placebo-Controlled Study to Assess the Efficacy of Twice-Daily Vardenafil in the Treatment of Lower Urinary Tract Symptoms Secondary to Benign Prostatic Hyperplasia
| Autor: | Ernst Ulbrich, Manfred Beneke, Christian G. Stief, Hartmut Porst, Dieter Neuser |
|---|---|
| Rok vydání: | 2008 |
| Předmět: |
Male
medicine.medical_specialty medicine.drug_mechanism_of_action Phosphodiesterase Inhibitors Urology Prostatic Hyperplasia Placebo-controlled study urologic and male genital diseases Placebo Drug Administration Schedule Piperazines Double-Blind Method Vardenafil Dihydrochloride Quality of life Lower urinary tract symptoms medicine Humans Sulfones Triazines business.industry Imidazoles Middle Aged medicine.disease Surgery Erectile dysfunction Vardenafil International Prostate Symptom Score business Prostatism Phosphodiesterase 5 inhibitor medicine.drug |
| Zdroj: | European Urology. 53:1236-1244 |
| ISSN: | 0302-2838 |
| DOI: | 10.1016/j.eururo.2008.01.075 |
| Popis: | Introduction Benign prostatic hyperplasia (BPH) is associated with bothersome lower urinary tract symptoms (LUTS) and reduced patient quality of life (QoL). Phosphodiesterase (type) 5 (PDE5) inhibitors such as vardenafil are commonly used for the treatment of erectile dysfunction (ED), but have also been shown to improve the symptoms of BPH. This randomised, double-blind, placebo-controlled study investigated the effects of vardenafil on LUTS and QoL in men with BPH/LUTS, with or without concomitant ED. Methods Men aged 45–64 yr with BPH/LUTS and an International Prostate Symptom Score (IPSS) ≥12 were randomised to receive either 10mg vardenafil or placebo twice daily. LUTS were assessed with the use of two primary efficacy parameters, IPSS score and maximum urinary flow rate (Q max ), as well as postvoid residual (PVR) urine volume; ED was measured with the use of the erectile function (EF) domain score of the International Index of Erectile Function (IIEF-EF); and QoL was assessed with the Urolife™ QoL-9 questionnaire. Results After 8 wk of treatment, there was a significant improvement in the IPSS total score in the vardenafil group compared with placebo (−5.9 and −3.6, respectively; p =0.0013). Nominally significant improvements in irritative and obstructive IPSS subscores ( p =0.0017 and p =0.0081, respectively), EF ( p =0.0001), and Urolife QoL-9 ( p max and PVR urine volume did not change significantly with treatment, although baseline values were already considered close to normal. Vardenafil was generally well tolerated, with most adverse events considered mild or moderate in severity. Conclusions Vardenafil treatment significantly improved LUTS, EF, and QoL in men with BPH/LUTS. Vardenafil may be considered a promising treatment option for men with symptoms secondary to BPH. |
| Databáze: | OpenAIRE |
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