一项多中心、随机、双盲、安慰剂对照试验,评估新型低剂量姜黄提取物配方对慢性膝关节疼痛健康成人的疗效和安全性。

IF 3.1 Q2 PHARMACOLOGY & PHARMACY
Clinical Pharmacology : Advances and Applications Pub Date : 2021-05-21 eCollection Date: 2021-01-01 DOI:10.2147/CPAA.S307464
Shefali Thanawala, Rajat Shah, Venkateswarlu Somepalli, KrishnaRaju Venkata Alluri, Prabakaran Desomayanandam, Arun Bhuvanendran
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引用次数: 0

摘要

背景:膝关节疼痛会导致功能受限,最终影响生活质量。我们评估了我们的水分散姜黄制剂(60% 天然姜黄素,TurmXTRA 60N®-WDTE60N)在缓解慢性膝关节疼痛症状方面的疗效:在这项随机、双盲、安慰剂对照试验中,受试者每天一次服用250毫克WDTE60N胶囊(150毫克姜黄素;53人)或外观匹配的安慰剂胶囊(53人),共服用90天。主要终点是80米快步行走测试后视觉模拟量表(VAS)上疼痛评分的变化:共有 96 名受试者完成了研究。从基线(5.4 ± 0.9)到第 90 天(3.8 ± 0.8),WDTE60N 可降低 VAS 评分,平均降低幅度大于安慰剂(-1.5 ± 0.7 vs -0.6 ± 0.8,p < 0.0001;2.5 倍)。与安慰剂相比,该药物还能明显缩短 80 米快步行走测试和 9 步爬楼梯测试所用时间,并改善所有生物标志物(p > 0.05)。发生了三起不良事件,但与研究产品无关:结论:WDTE60N 250 毫克,每天一次,连续服用 3 个月,可减轻慢性膝关节疼痛健康受试者的膝关节疼痛,改善关节功能,且耐受性良好,安全性高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial Assessing Efficacy and Safety of a Novel Low-Dose Turmeric Extract Formulation in Healthy Adults with Chronic Knee Pain.

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial Assessing Efficacy and Safety of a Novel Low-Dose Turmeric Extract Formulation in Healthy Adults with Chronic Knee Pain.

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial Assessing Efficacy and Safety of a Novel Low-Dose Turmeric Extract Formulation in Healthy Adults with Chronic Knee Pain.

Background: Knee pain causes functional limitations, eventually compromising the quality of life. We evaluated the efficacy of our water-dispersible turmeric formulation (60% natural curcuminoids, TurmXTRA 60N®-WDTE60N), which exhibited better PK profile at low dose (250 mg) than standard turmeric extract, in alleviating symptoms of chronic knee pain.

Methods: In this randomized, double-blind, placebo-controlled trial, subjects received either 250 mg WDTE60N capsule (150 mg curcuminoids; n = 53) or appearance-matched placebo capsule (n = 53) once daily for 90 days. Primary endpoint was change in pain score on the visual analogue scale (VAS) after 80-m fast-paced walk test.

Results: A total of 96 subjects completed the study. WDTE60N reduced VAS score from baseline (5.4 ± 0.9) to day 90 (3.8 ± 0.8) with greater mean reduction than placebo (-1.5 ± 0.7 vs -0.6 ± 0.8, p < 0.0001; 2.5 times). It also significantly improved the time taken for 80-m fast-paced walk test and 9-step stair-climb test; and improved all biomarkers compared to placebo (p > 0.05). Three adverse events occurred but were unrelated to study products.

Conclusion: WDTE60N 250 mg administered once daily for 3 months, alleviated knee pain, improved joint function in healthy subjects with chronic knee pain, was well tolerated and safe.

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来源期刊
CiteScore
4.60
自引率
0.00%
发文量
14
审稿时长
16 weeks
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