首页> 外文期刊>International journal of urology: official journal of the Japanese Urological Association >Can sildenafil treat primary premature ejaculation? A prospective clinical study.
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Can sildenafil treat primary premature ejaculation? A prospective clinical study.

机译:西地那非可以治疗原发性早泄吗?前瞻性临床研究。

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BACKGROUND: Recently, sildenafil has been demonstrated to be effective in treating premature ejaculation (PE). However, these studies ignored female factors and could not exclude the probability of drug interaction when combined with paroxetine. Therefore, the aim of this study was to evaluate the efficacy and safety of sildenafil alone in the treatment of primary PE, taking female factors into consideration. METHODS: One hundred and eighty potent men with primary PE were randomly divided into three groups and followed up for 6 months. Group A were treated with 50 mg sildenafil as needed, group B with 20 mg paroxetine daily and group C with squeeze technique daily. Intravaginal ejaculatory latency time (IELT), PE grade, intercourse satisfactory score (ISS), frequency of intercourse, and adverse effects of drugs were recorded before treatment, and 3 and 6 months after treatment. RESULTS: Compared with pretreatment, the three groups had significant differences in all the parameters after 3 or 6 months treatment, except the frequency of intercourse in Group C (all P = 0.00). However, there were no significant differences between 3 and 6 months. Compared with paroxetine and squeeze technique, after 3 or 6 months, sildenafil had significant differences in all the parameters (all P = 0.00). After 6 months, 1.7%, 18.3% and 36.7% patients in groups A, B and C, respectively, withdrew from the study and 86.7%, 60.0% and 45.0% patients, respectively, wanted to be treated further with the original administration, and this was statistically significant (both P = 0.00). CONCLUSION: Sildenafil is very effective and safe to treat PE, and has much higher efficacy than paroxetine and squeeze technique.
机译:背景:最近,西地那非已被证明可有效治疗早泄(PE)。但是,这些研究忽略了女性因素,不能排除与帕罗西汀联用时药物相互作用的可能性。因此,本研究的目的是评估西地那非单独治疗原发性PE的疗效和安全性,同时考虑女性因素。方法:将180名有力的原发性PE患者随机分为三组,并随访6个月。 A组根据需要用50 mg西地那非治疗,B组每天用20 mg帕罗西汀治疗,C组每天用挤压技术治疗。在治疗前,治疗后3个月和6个月记录阴道内射精潜伏时间(IELT),PE等级,性交满意评分(ISS),性交频率和药物不良反应。结果:与治疗前相比,三组在治疗3个月或6个月后所有参数均存在显着差异,除了C组的性交频率(所有P = 0.00)。但是,在3到6个月之间没有显着差异。与帕罗西汀和挤压技术相比,在3或6个月后,西地那非的所有参数均具有显着性差异(所有P = 0.00)。 6个月后,退出研究的A,B和C组分别有1.7%,18.3%和36.7%的患者退出研究,分别希望有86.7%,60.0%和45.0%的患者希望通过最初的给药方式进一步治疗,并且具有统计学意义(均P = 0.00)。结论:西地那非治疗PE非常有效且安全,比帕罗西汀和挤压技术具有更高的疗效。

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