Irvine Vascular Laboratories and Physiology, Department of Biomedical Sciences, Gabriele D'Annunzio University, Chieti-Pescara, Italy.
BJU Int. 2010 Oct;106(7):1030-3. doi: 10.1111/j.1464-410X.2010.09213.x. Epub 2010 Feb 22.
To assess the effects of a complex plant extract (Prelox®, a formulation of pine bark extract and l-arginine aspartate; Horphag Research UK Ltd, London, UK) on erectile dysfunction (ED) in men, as sexual desire typically persists in ageing men, while their erectile and endothelial function gradually declines.
In this double-blind, placebo-controlled study we assessed the effects of Prelox in 124 patients (aged 30-50 years) with moderate ED over an investigational period of 6 months. The International Index Of Erectile Function (IIEF) was used to quantify changes in sexual function.
The erectile domain of the IIEF (questions 1-5 plus 15) improved with Prelox from a baseline mean (sd) score of 15.2 (6.6) to 25.2 (2.1) after 3 months and 27.1 (2.1) after 6 months of treatment. In the placebo group there was an increase from a baseline score of 15.1 (7.0) to 19.1 (3.0) and 19.0 (3.1) after 3 and 6 months, respectively. The effects with Prelox were statistically significant compared with placebo (P < 0.05). Mean (SD) total plasma testosterone levels increased significantly from 15.9 (2.3) to 18.9 (2.6) nmol/L (P < 0.05) after 6 months with Prelox, compared to an increase from 16.9 (2.4) to 17.3 (2.3) nmol/L in the placebo group.
This study shows that Prelox is effective for improving erectile function, and that this effect persists on continuous therapy for up to 6 months. Moreover, there is some evidence that erectile function continues to improve the longer the therapy is used.
评估一种复杂植物提取物(Prelox®,由松树皮提取物和精氨酸天冬氨酸组成;Horphag Research UK Ltd,英国伦敦)对男性勃起功能障碍(ED)的影响,因为随着年龄的增长,男性的性欲通常会持续存在,而他们的勃起和内皮功能会逐渐下降。
在这项双盲、安慰剂对照的研究中,我们评估了 Prelox 在 124 名(年龄 30-50 岁)中度 ED 患者中的疗效,研究时间为 6 个月。国际勃起功能指数(IIEF)用于量化性功能的变化。
Prelox 治疗 3 个月后,IIEF 的勃起功能域(问题 1-5 加 15)从基线平均(标准差)评分 15.2(6.6)改善至 25.2(2.1),6 个月后改善至 27.1(2.1)。安慰剂组的基线评分从 15.1(7.0)增加至 19.1(3.0)和 19.0(3.1),分别在 3 个月和 6 个月后。与安慰剂相比,Prelox 的效果具有统计学意义(P < 0.05)。Prelox 治疗 6 个月后,总血浆睾酮水平从 15.9(2.3)升高至 18.9(2.6)nmol/L(P < 0.05),而安慰剂组从 16.9(2.4)升高至 17.3(2.3)nmol/L。
这项研究表明,Prelox 可有效改善勃起功能,且连续治疗长达 6 个月时效果持续存在。此外,有证据表明,治疗时间越长,勃起功能继续改善。