Phytotherapy of Male Hypoactive Sexual Desire of Psychogenic Origin: A Preliminary Study

G. Cavallini, G. Biagiotti
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Abstract

This is a prospective placebo-controlled study to test the efficacy and safety of a dietary supplement (Vigoryx®, FG. -Pharma, Rome-Italy) for men with Psychogenic Hypoactive Sexual Desire (pHSD). The composition of Vigoryx was as follows: selenium 55 mg, L-Carnitine 250 mg, red ginseng 135 mg, aframomum 20 mg and eruca 300 mg. This is a two-center prospective blind placebo-controlled study. All patients affected by pHSD were considered to be candidates. Sexual desire was assessed in each patient before and after active drug or placebo administration using the International Index of Erectile Function (IIEF15, items 11 and 12) and Patient Global Impression of Improvement (PGI-I, seven grade scale) scores. The patients received Vigoryx® (active drug, Group 1) or a control substance (alimentary starch, Group 2). The differences between the unmatched groups were assessed using the Mann-Whitney Rank test, and the differences between before and after (matched groups) therapy were assessed using the Wilcoxon Signed Rank test. The side effects were compared between the two groups using the chi2 test. Eighty-four patients were studied. Forty patients used Vigoryx (Group 1), and 44 used a placebo (Group 2). No significant differences existed between the basal IIEF scores, and between the basal scores and the score achieved after a three-month administration of the control substance; on the other hand, the IIEF score after a three-month administration of Vigoryx was significantly higher than the basal scores and the score achieved after control substance administration. Furthermore, the PGI-I score achieved after active drug administration was significantly higher than the PGI-I score achieved after starch administration. No side effects emerged in either group. Vigoryx is a safe and efficient drug for the treatment of pHSD.
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植物治疗男性心因性性欲减退的初步研究
这是一项前瞻性安慰剂对照研究,旨在测试一种膳食补充剂(Vigoryx®,FG)的疗效和安全性。(罗马-意大利制药公司),用于治疗心因性性欲减退(pHSD)的男性。其组成为:硒55 mg,左旋肉碱250 mg,红参135 mg,金针菇20 mg,云雀300 mg。这是一项双中心前瞻性盲安慰剂对照研究。所有受博士学位影响的患者都被认为是候选人。使用国际勃起功能指数(IIEF15,第11项和第12项)和患者整体改善印象(pgi - 1, 7级量表)评分评估每位患者在服用活性药物或安慰剂前后的性欲。患者接受Vigoryx®(活性药物,第1组)或对照物质(消化淀粉,第2组)治疗。未匹配组之间的差异采用Mann-Whitney Rank检验评估,(匹配组)治疗前后的差异采用Wilcoxon sign Rank检验评估。采用chi2检验比较两组的副作用。84例患者接受了研究。40名患者使用Vigoryx(第一组),44名患者使用安慰剂(第二组)。基础IIEF评分之间以及基础评分与服用对照物质三个月后获得的评分之间没有显著差异;另一方面,服用Vigoryx三个月后的IIEF评分显著高于基础评分和服用对照物质后的评分。此外,活性药物给药后的PGI-I评分显著高于淀粉给药后的PGI-I评分。两组均未出现副作用。Vigoryx是一种安全有效的治疗pHSD的药物。
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