首页> 外文期刊>The Journal of Urology >Treatment of premature ejaculation with sertraline hydrochloride: a single-blind placebo controlled crossover study.
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Treatment of premature ejaculation with sertraline hydrochloride: a single-blind placebo controlled crossover study.

机译:盐酸舍曲林治疗早泄:单盲安慰剂对照研究。

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PURPOSE: The efficacy of sertraline hydrochloride for the treatment of premature ejaculation is evaluated. MATERIALS AND METHODS: A total of 37 potent men, 19 to 70 years old (mean age 41), with premature ejaculation were treated with 50 mg. oral sertraline and placebo in a controlled randomized single-blind crossover trial. All men were either married or in a stable relationship. None of the patients received any formal psychosexual therapy. Chronic open label treatment with sertraline was continued in 29 patients who had achieved an increase in ejaculatory latency times over pretreatment levels with active drug in the initial crossover study. In an attempt to identify which patients could maintain the improved ejaculatory control after withdrawal of the active drug, serial drug withdrawal was conducted every 4 weeks with drug initiation after a further 2 weeks if improved ejaculatory control was not maintained. RESULTS: The mean pretreatment ejaculatory latency time was 0.3 minute (range 0 to 1). The mean ejaculatory interval after 4 weeks of treatment was 3.2 minutes (range 1 minute to anejaculation) with sertraline and 0.5 minute (range 0 to 1) with placebo (p <0.001). Intravaginal ejaculation was achieved for the first time in 5 patients with primary premature ejaculation and 2 patients experienced anejaculation. One patient described minor drowsiness and anorexia, and 2 patients described mild, transient gastrointestinal upset. Staged drug withdrawal allowed 20 of the 29 patients (67%) on chronic open label treatment with sertraline to discontinue the drug after a mean interval of 7.3 months with a mean ejaculatory latency time of 4.1 minutes (range 1 to 12). CONCLUSIONS: Sertraline appears to be a useful agent in the pharmacological treatment of premature ejaculation.
机译:目的:评估盐酸舍曲林治疗早泄的疗效。材料与方法:总计37名19至70岁(平均年龄41岁)有力射精的男性,接受早泄治疗,剂量为50 mg。口服舍曲林和安慰剂在一项受控的随机单盲交叉试验中。所有男人都已结婚或处于稳定的关系。没有患者接受任何正式的心理治疗。在最初的交叉研究中,有29名患者继续接受舍曲林的慢性开放标签治疗,这些患者的射精潜伏期时间超过了使用活性药物治疗前水平。为了确定退出活性药物后哪些患者可以维持改善的射精控制,如果不能维持改善的射精控制,则每隔4周进行一次连续的药物退出,并在开始2周后再开始用药。结果:平均治疗前射精潜伏时间为0.3分钟(范围为0到1)。舍曲林治疗4周后的平均射精间隔为3.2分钟(射精为1分钟),安慰剂为0.5分钟(0至1)(p <0.001)。 5例原发性早泄和2例经历了射精的患者首次实现了阴道内射精。 1名患者描述了轻微的嗜睡和厌食,2名患者描述了轻度暂时性胃肠道不适。分阶段撤药允许使用舍曲林进行慢性开放标签治疗的29例患者中的20例(67%)在平均间隔7.3个月后平均射精潜伏时间为4.1分钟(范围为1至12)而停药。结论:舍曲林似乎是治疗早泄的有用药物。

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