Haghighi Mohammad, Doostizadeh Mona, Jahangard Leila, Soltanian Alireza, Faryadres Mohammad, Dürsteler Kenneth M, Beatrix Brühl Annette, Sadeghi-Bahmani Dena, Brand Serge
Behavioral Disorders and Substance Abuse Research Center, Hamadan University of Medical Sciences, Hamadan 6516848741, Iran.
Modeling of Non-Communicable Diseases Research Center, Hamadan University of Medical Sciences, Hamadan 6516848741, Iran.
Healthcare (Basel). 2021 Jul 7;9(7):859. doi: 10.3390/healthcare9070859.
Among male sexual dysfunctions, erectile dysfunction and early ejaculation have the highest prevalence rates. Here, we tested the influence of lisdexamfetamine dimesylate (Vyas) on early ejaculation. To this end, we performed a double-blind randomized clinical trial among males with early ejaculation.
A total of 46 males with early ejaculation (mean age: 35.23 years) and in stable marital relationships with regular weekly penile-vaginal intercourse were randomly assigned either to the lisdexamfetamine dimesylate condition (30 mg) or to the placebo condition. Compounds were taken about six hours before intended penile-vaginal intercourse. At baseline and four weeks later at the end of the study, participants completed a series of self-rating questionnaires covering early ejaculation. Female partners also rated participants' early ejaculation profile.
Compared to the placebo condition, dimensions of early ejaculation improved over time in the lisdexamfetamine condition, though improvements were also observed in the placebo condition.
Among male adults in stable marital relationships with regular weekly penile-vaginal intercourse, lisdexamfetamine dimesylate improved dimensions of early ejaculation. Given that improvements were also observed in the placebo condition, psychological factors such as increased attention to early ejaculation and favorable expectations of the compound should be considered.
在男性性功能障碍中,勃起功能障碍和早泄的患病率最高。在此,我们测试了二甲磺酸赖右苯丙胺(Vyas)对早泄的影响。为此,我们对患有早泄的男性进行了一项双盲随机临床试验。
共有46名患有早泄的男性(平均年龄:35.23岁),婚姻关系稳定,每周有规律地进行阴茎-阴道性交,他们被随机分配到二甲磺酸赖右苯丙胺组(30毫克)或安慰剂组。药物在预期的阴茎-阴道性交前约6小时服用。在基线时以及研究结束四周后,参与者完成了一系列涵盖早泄的自评问卷。女性伴侣也对参与者的早泄情况进行了评分。
与安慰剂组相比,二甲磺酸赖右苯丙胺组早泄的各项指标随时间有所改善,不过安慰剂组也有改善。
在婚姻关系稳定、每周有规律地进行阴茎-阴道性交的成年男性中,二甲磺酸赖右苯丙胺改善了早泄的各项指标。鉴于安慰剂组也观察到了改善情况,应考虑诸如对早泄关注度增加以及对该药物的良好预期等心理因素。