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Effects of Herbal vigRX on Premature Ejaculation: A randomized, double-blind study

机译:草药vigRX对早泄的影响:一项随机双盲研究

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ObjectiveWe conducted a double-blind, placebo-controlled study to determine the efficacy of an herbal sexual supplement (vigRX) on premature ejaculation (PE).MethodA randomized double blind study was conducted on a fixed dose of herbal vigRX at Roozbeh Psychiatry Hospital, Tehran University of Medical Sciences. The sample consisted of 85 married patients diagnosed with primary PE according to Diagnostic and Statistical Manual of Mental Disorders. Each patient underwent diagnostic evaluation by one trained psychiatrist, using Structured Clinical Interview for DSM-IV-TR. Each patient was evaluated by researchers to exclude the organic sexual dysfunctions. The patients were randomly assigned in to two groups: group 1 consisting of 42 patients receiving placebo, and group 2 consisting of 43 patients receiving 540 mg herbal vigRX for a 4-week treatment course. The effects of the drug on the ejaculatory function in each group were assessed by the intravaginal ejaculation latency time (IELT), and the Chinese Index of Premature Ejaculation (CIPE) before and at the end of the treatment course. Statistical analysis was performed using SPSS software (15th version).ResultsThe mean IELT increased 22.4 and 32.0 seconds in the placebo and the vigRX group respectively after the treatment course. The mean IELT differences between the two groups was not significant. The mean CIPE score increased 2.40 and 4.37 in the placebo and the vigRX group respectively. The mean CIPE score differences between the two groups was not significant.No side effect was reported by the subjects in neither groups during the treatment course.ConclusionAlthough the improvement in IELT and CIPE scores in the herbal vigRX group was more than the placebo group, this difference was not statistically significant. The increasing of IELT and CIPE score in the placebo group may be due to the placebo effects. Further studies with higher vigRX doses, greater sample size and longer treatment courses are warranted.
机译:目的我们进行了一项双盲,安慰剂对照研究,以确定草药性补充剂(vigRX)对早泄(PE)的疗效。方法在德黑兰州罗兹比精神病医院对固定剂量的草药vigRX进行了随机双盲研究。医科大学。该样本包括根据《精神障碍诊断和统计手册》诊断为原发性PE的85位已婚患者。使用DSM-IV-TR的结构化临床访谈,每位患者均由一名训练有素的精神科医生进行诊断评估。研究人员对每位患者进行了评估,以排除器质性功能障碍。将患者随机分为两组:第1组由42位接受安慰剂的患者组成,第2组由43位接受540 mg草药vigRX的患者组成,为期4周。通过治疗前和治疗结束时的阴道内射精潜伏时间(IELT)和中国早泄指数(CIPE)评估药物对各组射精功能的影响。使用SPSS软件(第15版)进行统计分析。结果疗程结束后,安慰剂组和vigRX组的平均IELT分别增加了22.4和32.0秒。两组之间的平均IELT差异不显着。安慰剂组和vigRX组的CIPE平均得分分别提高了2.40和4.37。两组之间的平均CIPE评分差异不显着,在治疗过程中两组均未见副作用的报道。结论尽管vigRX组的IELT和CIPE评分的改善程度大于安慰剂组,但差异无统计学意义。安慰剂组中IELT和CIPE评分的升高可能是由于安慰剂的作用。更高的vigRX剂量,更大的样本量和更长的治疗疗程值得进一步研究。

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