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On-demand Take of Dapoxetine for the Treatment of Lifelong Premature Ejaculation: Prospective, Randomized, Placebo Controlled Study

机译:按需服用Dakoxetine治疗终身早泄:前瞻性,随机,安慰剂对照研究

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The objective of this study is to assess the safety and efficacy of on-demand use of dapoxetine intreating lifelong premature ejaculation. This is a prospective, single center, single blind, placebo controlled study. During the period of months between january 2015 and july 2015, 60 patients diagnosed with lifelong premature ejaculation (LPE) in outpatient department of China and Japan Union Hospital Of Jilin University, were randomized to receive different sequences of the two medications equally: placebo(group A), 30mg or 60mg of dapoxetine(group B) according to the efficacy at 8th week. Every patient received each medication for 12 weeks. Intravaginal ejaculatory latency time (IELT), premature ejaculation diagnostic tools (PEDT) score, sexual satisfaction score of patients and sexual partners were recorded during the study period. Successful of LPE is defined whether IELT exceed 120s. Meanwhile we observed the occurrence of adverse events in two groups. 55 patients enrolled in our study completed the study overl2 weeks, 27 cases receive placebo and 28 cases receive 30mg or 60mg dapoxetine. Patients in group B had a significantly longer mean IELT than group A(120.4s vs 42.1s, P<0.01). The average PEDT score in group B was different with group A(9.9 vs 13.7, P<0.01). Both of patients and sexual partners in group B felt more satisfied with their sexual life, which were better than group A(3.1 vs 1.8,2.8 vs 1.9, respectively, P<0.01). 3 cases appeared dizziness and 1 case appeared nausea. There was no serious adverse event in any subjects. On-demand use of dapoxetine may be considered a safe and effective way in treating lifelong premature ejaculation. The long-term benefits need further study.
机译:本研究的目的是评估按需使用Dakoxetine inteling终身射精的安全性和有效性。这是一个预期,单中心,单盲,安慰剂对照研究。在2015年1月至2015年7月期间的几个月内,吉林大学外科医院外科医院患有终身射精(LPE)的60名患者随机地接受两种药物的不同序列:安慰剂(集团a),根据第8周的疗效,30mg或60mg Dakoxetine(B组)。每只患者都接受了每种药物12周。在研究期间,记录了气体射精延迟时间(IELT),早泄诊断工具(PEDT)评分,患者和性伴侣的性满足评分。 LPE的成功定义了是否超过120岁。同时,我们观察了两组不良事件的发生。 55例患者参加我们的研究完成了研究叠加2周,27例接受安慰剂和28例,接受30mg或60mg百兆汀。 B组患者比A组(120.4s与42.1s,P <0.01)有明显更长的平均值。 B组的平均Pedt评分与A组(9.9 Vs 13.7,P <0.01)不同。 B组的患者和性伴侣都对其性生活感到满意,比A组优于A(3.1 Vs 1.8,2.8 Vs 1.9,P <0.01)。 3例出现头晕,1例出现恶心。任何科目都没有严重的不良事件。在治疗终身早熟射精时,按需使用脂氧化汀的使用可能被认为是一种安全有效的方法。长期效益需要进一步研究。

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