Suppr超能文献

一项双盲、随机、安慰剂对照研究,评估穿心莲标准化提取物(ParActin®)对膝骨关节炎患者减轻疼痛的疗效。

A double-blind, randomized, placebo-controlled study to assess the efficacy of Andrographis paniculata standardized extract (ParActin®) on pain reduction in subjects with knee osteoarthritis.

机构信息

HPIngredients, Bradenton, Florida.

Clinical Development, Vedic Lifesciences Pvt Ltd, Mumbai, Maharashtra, India.

出版信息

Phytother Res. 2019 May;33(5):1469-1479. doi: 10.1002/ptr.6339. Epub 2019 Apr 10.

Abstract

Andrographis paniculata Wall (Acanthaceae) is becoming more recognized for its anti-inflammatory and antioxidant properties. A randomized, double-blind, placebo-controlled study was conducted to assess the efficacy of an andrographolide-containing supplement, ParActin® (300 and 600 mg daily), on Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) pain reduction in patients with knee osteoarthritis. Joint stiffness, physical function, changes in the SF-36 quality of life questionnaire, a fatigue scale, and safety were also evaluated. A total of 103 male and female patients with I-II osteoarthritis of the knee joint were assessed. Patients treated with 300 or 600 mg/day of ParActin® showed a significant reduction in pain at days 28, 56, and 84 compared with a placebo group. WOMAC stiffness scores, physical function score, and the fatigue score showed a significant improvement in both ParActin®-treated groups compared with the placebo group. At the end of the study, the quality of life (SF-36 questionnaire) and Functional Assessment of Chronic Illness Therapy (FACIT) scores showed significant improvements in both ParActin®-treated groups compared with the placebo group. Overall, it can be concluded that ParActin® in 300 and 600 mg/day dosages were found to be effective and safe in reducing pain in individuals suffering from mild to moderate knee osteoarthritis.

摘要

穿心莲(爵床科)因其具有抗炎和抗氧化特性而越来越受到认可。一项随机、双盲、安慰剂对照研究评估了含有穿心莲内酯的补充剂 ParActin®(每天 300 和 600 毫克)对膝骨关节炎患者的 Western Ontario 和 McMaster 大学骨关节炎指数(WOMAC)疼痛减轻的疗效。关节僵硬、身体功能、SF-36 生活质量问卷变化、疲劳量表以及安全性也进行了评估。共有 103 名男性和女性 I-II 期膝关节骨关节炎患者接受了评估。与安慰剂组相比,每天服用 300 或 600 毫克 ParActin®的患者在第 28、56 和 84 天疼痛明显减轻。在 ParActin®治疗组中,WOMAC 僵硬评分、身体功能评分和疲劳评分均较安慰剂组显著改善。在研究结束时,生活质量(SF-36 问卷)和慢性疾病治疗功能评估(FACIT)评分显示,与安慰剂组相比,ParActin®治疗组均有显著改善。总的来说,可以得出结论,每天服用 300 和 600 毫克的 ParActin®在减轻轻度至中度膝骨关节炎患者的疼痛方面是有效且安全的。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验