首页> 美国卫生研究院文献>Asian Journal of Andrology >An open comparative multicentre clinical study of combined oral therapy with sildenafil and doxazosin GITS for treating Chinese patients with erectile dysfunction and lower urinary tract symptoms secondary to benign prostatic hyperplasia
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An open comparative multicentre clinical study of combined oral therapy with sildenafil and doxazosin GITS for treating Chinese patients with erectile dysfunction and lower urinary tract symptoms secondary to benign prostatic hyperplasia

机译:西地那非联合多沙唑嗪GITS联合口服治疗开放性比较性多中心临床研究治疗中国继发于前列腺增生的勃起功能障碍和下尿路症状的中国患者

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摘要

This study sought to investigate the clinical efficacy and safety of combined oral therapy with sildenafil and doxazosin GITS compared to sildenafil monotherapy in treating Chinese patients with erectile dysfunction (ED) and lower urinary tract symptoms secondary to benign prostatic hyperplasia (BPH/LUTS). The trial was conducted in hospitals in Beijing, Shanghai, Changsha, Wuhan and Guangzhou, five major cities in China. A total of 250 patients diagnosed with ED and BPH/LUTS aged 50–75 years, and who had International Index of Erection Function-5 (IIEF-5) scores ≤21 and International Prostate Symptom Score (IPSS) ≥10 points, were enrolled and randomly divided into Group A (168 cases; doxazosin GITS 4 mg once daily plus sildenafil 25–100 mg on demand) and Group B (82 cases; sildenafil 25–100 mg on demand). Efficacies were evaluated by IIEF-5 and IPSS scores and a quality of life (QoL) questionnaire, and adverse effects were evaluated during the treatment period. There were no statistically significant differences in mean age, and IIEF-5, IPSS and QoL scores pre-treatment between the two groups. After treatment, IIEF-5, IPSS and QoL scores were significantly improved in Group A, while only IIEF-5 scores were significantly improved in Group B compared with pre-treatment. There were no significant differences in side effects between the two groups. The results indicated that combined therapy with sildenafil and doxazosin GITS for the treatment of ED and BPH/LUTS is safe and effective compared to sildenafil monotherapy.
机译:本研究旨在探讨西地那非和多沙唑嗪GITS联合口服治疗与西地那非单药治疗在治疗患有良性前列腺增生(BPH / LUTS)的勃起功能障碍(ED)和下尿路症状的中国患者中的临床疗效和安全性。该试验在中国五个主要城市的北京,上海,长沙,武汉和广州的医院中进行。共有250名诊断为ED和BPH / LUTS的年龄在50-75岁且国际勃起功能指数5(IIEF-5)得分≤21和国际前列腺症状得分(IPSS)≥10分的患者入选。并随机分为A组(168例;多沙唑嗪GITS 4 mg,每天一次,加西地那非25–100 mg,按需)和B组(82例,西地那非25–100 mg,按需)。通过IIEF-5和IPSS评分以及生活质量(QoL)问卷评估疗效,并在治疗期间评估不良反应。两组之间的平均年龄,IIEF-5,IPSS和QoL评分在治疗前均无统计学差异。与治疗前相比,治疗后,A组的IIEF-5,IPSS和QoL得分明显提高,而B组中只有IIEF-5得分显着提高。两组之间的副作用无显着差异。结果表明,与西地那非单药治疗相比,西地那非与多沙唑嗪GITS联合治疗ED和BPH / LUTS安全有效。

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