Caruso Salvatore, Intelisano Giorgia, Farina Marco, Di Mari Lucia, Agnello Carmela
Section of Gynecology, Department of Microbiological Science and Gynecological Science, School of Medicine, University of Catania, Ospedale S. Bambino, Catania, Italy.
Eur J Obstet Gynecol Reprod Biol. 2003 Oct 10;110(2):201-6. doi: 10.1016/s0301-2115(03)00118-0.
To determine the changes, if any, on female sexual pathways using sildenafil (primary outcome), and to verify the safety of this drug (second outcome).
Following previous research on symptomatic women, we wanted to study the effects of sildenafil on asymptomatic women. We would like to make it clear from the outset that this study is part of an ongoing line of research and this drug, and others of its type, should be used under strict medical supervision only on symptomatic patients. A randomized double-blind cross-over, placebo-controlled study was conducted at the Family Planning Centre of the Group for Sexological Research, Department of Microbiological and Gynecological Science, School of Medicine, University of Catania, Italy. Sixty-eight healthy volunteer women aged 19-38 years, asymptomatic for sexual disorders, were enrolled. The study consisted of 4 weeks sildenafil, 2 weeks washout, and 4 weeks placebo, by two possible sequences: sildenafil 50 mg, washout, placebo; or placebo, washout, sildenafil 50 mg. Efficacy of sildenafil was assessed by the Personal Experiences Questionnaire (PEQ) based on the 5-point Likert scale. The questionnaire quantified subjective sexual aspects at baseline, during washout, after treatments, and at the follow-ups. Statistical analysis was done with the Wilcoxon's rank-sum test and Student's t-test.
50/68 women completed the study at the first follow-up, and 38 women reached the second follow-up. Six women withdrew because of adverse events. Sildenafil improved arousal (P<0.001), orgasm (P<0.05), and enjoyment (P<0.001) with respect to placebo. Significant differences were noted during sildenafil usage with respect to the baseline for arousal (P<0.01), orgasm (P<0.001), and sexual enjoyment (P<0.001). The adverse events were transient and mild or moderate.
Our study suggests that sildenafil acts on the different sexual pathways in healthy women, improving their sexual experience. This study could help to understand the physiologic and pathophysiologic aspects of female sexuality. In comparison with current psychosexual therapies, which are long-term, compliance would be improved with use of this drug. Additional studies are required to define the use of sildenafil in a clinical setting.
确定使用西地那非(主要结局)对女性性途径的影响(若有),并验证该药物的安全性(次要结局)。
在先前对有症状女性进行研究之后,我们想研究西地那非对无症状女性的影响。我们想从一开始就明确,本研究是正在进行的一系列研究的一部分,这种药物以及其他同类药物仅应在严格的医学监督下用于有症状的患者。在意大利卡塔尼亚大学医学院微生物学与妇科科学系性学研究小组计划生育中心进行了一项随机双盲交叉、安慰剂对照研究。招募了68名年龄在19 - 38岁、无性功能障碍症状的健康志愿者女性。该研究包括4周的西地那非治疗、2周的洗脱期和4周的安慰剂治疗,有两种可能的顺序:西地那非50毫克、洗脱期、安慰剂;或安慰剂、洗脱期、西地那非50毫克。通过基于5点李克特量表的个人体验问卷(PEQ)评估西地那非的疗效。该问卷对基线、洗脱期、治疗后以及随访时的主观性方面进行了量化。采用威尔科克森秩和检验和学生t检验进行统计分析。
68名女性中有50名在首次随访时完成了研究,38名女性进入了第二次随访。6名女性因不良事件退出。与安慰剂相比,西地那非改善了性唤起(P<0.001)、性高潮(P<0.05)和性快感(P<0.001)。在使用西地那非期间,与基线相比,性唤起(P<0.01)、性高潮(P<0.001)和性快感(P<0.001)有显著差异。不良事件是短暂的,且为轻度或中度。
我们的研究表明,西地那非作用于健康女性的不同性途径,改善她们的性体验。本研究有助于了解女性性生理和病理生理方面。与目前长期的性心理治疗相比,使用这种药物可提高依从性。需要进一步研究来确定西地那非在临床环境中的应用。