Safety and efficacy of LibidUp-PE supplement on premature ejaculation: A randomized, placebo-controlled double-blind, crossover study

Jagadeesan M , Adhisaya A , T. Srinivasan , Alphienes Stanley Xavier , Pavithra Anandan , Rajappan Chandra Satish Kumar , Thangavel Mahalingam Vijayakumar
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Abstract

Premature ejaculation (PE) is the most common male sexual dysfunction. Selective serotonin reuptake inhibitors (SSRIs) are currently recommended for PE. However, the side effects of SSRIs, such as nausea, vomiting, and xerostomia, pose challenges to clinicians. Simultaneously, evidence indicates that psychological and behavioral treatments are often insufficient. LibidUp-PE is a nutraceutical designed to enhance sexual wellness and contains a combination of essential amino acids to boost stamina and vigor, addressing concerns like erectile dysfunction (ED). This study aimed to assess the safety and efficacy of LibidUp-PE in the treatment of PE. In this crossover, double-blind, placebo-controlled trial, 76 patients with PE were randomly divided into two groups. Group A received LibidUp-PE, whereas Group B received a placebo for 12 weeks. Following a 2-week wash-out period, the groups switched treatments for another 12 weeks. Intravaginal ejaculatory latency time (IELT) and post-ejaculatory refractory time (PERT) were measured as the primary outcomes to evaluate PE improvement. Plasma serotonin levels were measured as secondary parameters using enzyme-linked immunosorbent assay. The results showed that LibidUp-PE significantly improved the IELT score, increasing from 0.8 ± 0.2 min to 2.9 ± 1.1 min (p < 0.01). PERT scores also significantly decreased from 15.8 ± 1.7 min to 5.6 ± 0.6 min after 12 weeks of LibidUp-PE treatment. Plasma serotonin levels significant increased from 93.6 ± 7.8 ng/mL to 168.4 ± 12.8 ng/mL (p < 0.001) with LibidUp-PE treatment. In contrast, no significant improvements were observed in the placebo group. Notably, none of the participants withdrew their consent due to adverse reactions, which is indicative of the safety and tolerability of LibidUp-PE. In conclusion, 12-week treatment with LibidUp-PE demonstrated a beneficial effect in reducing PE symptoms, as reflected by improved IELT, reduced PERT, and increased plasma serotonin levels. Therefore, LibidUp-PE could be a promising solution for individuals with PE.

LibidUp-PE补充剂对早泄的安全性和有效性:随机、安慰剂对照、双盲、交叉研究
早泄(PE)是最常见的男性性功能障碍。选择性血清素再摄取抑制剂(SSRIs)是目前治疗早泄的推荐药物。然而,SSRIs 的副作用,如恶心、呕吐和口干舌燥,给临床医生带来了挑战。同时,有证据表明,心理和行为治疗往往是不够的。LibidUp-PE是一种旨在提高性健康的营养保健品,含有多种必需氨基酸,可增强耐力和活力,解决勃起功能障碍(ED)等问题。这项研究旨在评估 LibidUp-PE 治疗 PE 的安全性和有效性。在这项交叉、双盲、安慰剂对照试验中,76 名 PE 患者被随机分为两组。A组接受LibidUp-PE治疗,B组接受为期12周的安慰剂治疗。在2周的冲洗期后,两组互换治疗方法,再进行12周的治疗。阴道内射精潜伏时间(IELT)和射精后难射精时间(PERT)是评估PE改善情况的主要结果。使用酶联免疫吸附试验测量血浆血清素水平作为次要参数。结果显示,LibidUp-PE明显改善了IELT评分,从0.8±0.2分钟增加到2.9±1.1分钟(p <0.01)。经过12周的LibidUp-PE治疗后,PERT评分也从15.8±1.7分明显降低到5.6±0.6分。LibidUp-PE治疗后,血浆血清素水平从93.6 ± 7.8 ng/mL显著增加到168.4 ± 12.8 ng/mL(p < 0.001)。相比之下,安慰剂组没有观察到明显改善。值得注意的是,没有一位参与者因不良反应而撤回同意书,这表明了LibidUp-PE的安全性和耐受性。总之,LibidUp-PE为期12周的治疗在减轻PE症状方面表现出了有益的效果,这体现在IELT的改善、PERT的降低和血浆5-羟色胺水平的提高上。因此,LibidUp-PE 对 PE 患者来说是一种很有前景的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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