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Treatment of Patients with Erectile Dysfunction by Shugan Yiyang Capsule: Multi-Centered Randomized Controlled Trial

机译:疏肝益阳胶囊治疗勃起功能障碍患者的多中心随机对照试验

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Objective: To evaluate the efficacy and safety of Shugan Yiyang Capsule (SGYY) in treating psychogenic and mild arteriogenic erectile dysfunction (ED) of Gan stagnation and Shen deficiency Syndrome type with or without blood stasis. Methods: A multi-centered, randomized, double-blinded, placebo-controlled trial in 304 patients was conducted by dividing them into 3 groups, who received respectively SGYY (n = 102), placebo (n = 101) and Suoyang Bushen capsule (SYBS, n = 101), 1. 0g taken three times a day for 4 weeks. Besides, 205 patients were arranged in an open-label study and treated with SGYY 1. 0g taken three times a day for 4 weeks. The total effective rate, total remarkably effective rate, erection recovery rate tested by penis hardness test ring, time taken for improving erection a-mong groups, as well as therapeutic effect between psychogenic ED group and mild arteriogenic ED group were compared. Adverse reactions related to SGYY were recorded. And a 3-month follow-up study was conducted on 105 cured patients. Results: The trial was completed in 500 patients. The total effective rate and total remarkably effective rate in the SGYY treated double-blinded group were 88. 0% and 64. 0% respectively, and those in the open-label group 90. 5% and 65.0% , respectively, all significantly higher than those in the placebo (21.0%, 6.0%) and SYBS groups (60. 0% , 29.0%), P<0.01. At the same time, the e-rection recovery rate and improving time in SGYY group were significantly better than those in other groups (P<0. 01). No adverse reactions related to SGYY were found. The successful rate of potency to have intercourse within 3 months was over 80% (100 patients out of the 105 cured patients). Conclusion: SGYY was an effective and safe treatment for patients with psychogenic and mild arteriogenic ED of Gan stagnation and Shen deficiency Syndrome type with or without blood stasis, especially for psychogenic ED patients.
机译:目的:评价疏肝益阳胶囊(SGYY)治疗肝郁血瘀证型和轻度血瘀型精神病性和轻度勃起功能障碍(ED)的疗效和安全性。方法:对304例患者进行多中心,随机,双盲,安慰剂对照试验,将其分为3组,分别接受SGYY(n = 102),安慰剂(n = 101)和锁阳补肾胶囊( SYBS,n = 101),每天1次。0g,连续3周,共4周。此外,有205名患者被安排在一项开放标签研究中,并接受SGYY 1治疗。每天3次服用0g,共4周。比较总有效率,总有效率,通过阴茎硬度测试环测得的勃起恢复率,改善勃起a-mong组所花费的时间以及心因性ED组和轻度动脉源性ED组之间的治疗效果。记录与SGYY相关的不良反应。并对105例治愈的患者进行了为期3个月的随访研究。结果:该试验在500例患者中完成。 SGYY治疗的双盲组的总有效率和显着总有效率分别为88. 0%和64. 0%,而开放标签组分别为90. 5%和65.0%。与安慰剂组(21.0%,6.0%)和SYBS组(60. 0%,29.0%)相比,P <0.01。同时,SGYY组的勃起恢复率和改善时间明显优于其他组(P <0。01)。未发现与SGYY相关的不良反应。 3个月内性交成功的成功率超过80%(105名治愈患者中有100名患者)。结论:SGYY是一种治疗心绞痛,轻度动脉粥样硬化性肝郁血沉,肾虚证型及无血瘀型患者的有效,安全的方法,特别是对于精神病性ED患者。

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