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一项开放标签的为期六个月的扩展研究,旨在调查青蒿提取物用于治疗与髋膝骨关节炎相关的疼痛、僵硬和功能受限的安全性和有效性。

An open-label six-month extension study to investigate the safety and efficacy of an extract of Artemisia annua for managing pain, stiffness and functional limitation associated with osteoarthritis of the hip and knee.

作者信息

Hunt Sheena, Stebbings Simon, McNamara Debra

机构信息

Principal Scientist, Promisia Ltd, Wellington.

Associate Professor in Medicine, Rheumatology Research Unit, Department of Medicine, Dunedin School of Medicine, University of Otago, Dunedin.

出版信息

N Z Med J. 2016 Oct 28;129(1444):97-102.

Abstract

AIMS

This six-month single-centre open-label extension study, conducted at the University of Otago, Dunedin, follows from a previously published 12-week pilot double-blind randomised placebo-controlled study of dietary supplement, Arthrem® (ART) in patients with osteoarthritis (OA) of the hip or knee. The pilot double-blind study showed that treatment with ART 150 mg twice-daily was associated with clinically relevant pain reduction. The extension study aims were to assess longer-term safety and efficacy during six months' treatment following the pilot trial.

METHOD

Patients who completed the pilot double-blind study had the option to continue on open-label treatment with ART for a further six months. Safety was assessed by adverse event monitoring and laboratory tests at three and six months. Efficacy was assessed at three and six months using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC®).

RESULTS

Thirty-four patients entered the optional extension and 28 completed six months' treatment. ART was well tolerated when taken for up to nine months. Improvements in WOMAC® efficacy parameters reported in the double-blind phase of the study were maintained over six months.

CONCLUSION

ART appears to be a safe and effective alternative for managing the symptoms of OA over an extended period.

摘要

目的

这项为期六个月的单中心开放标签扩展研究在达尼丁的奥塔哥大学进行,它是基于之前发表的一项为期12周的膳食补充剂Arthrem®(ART)治疗髋或膝骨关节炎(OA)患者的双盲随机安慰剂对照试验。该双盲试验表明,每日两次服用150毫克ART与临床上显著的疼痛减轻相关。扩展研究的目的是评估在先导试验后的六个月治疗期间的长期安全性和疗效。

方法

完成先导双盲研究的患者可以选择继续接受ART的开放标签治疗,为期六个月。通过在三个月和六个月时监测不良事件和进行实验室检查来评估安全性。在三个月和六个月时使用西安大略和麦克马斯特大学骨关节炎指数(WOMAC®)评估疗效。

结果

34名患者进入了可选的扩展阶段,28名患者完成了六个月的治疗。ART服用长达九个月时耐受性良好。研究双盲阶段报告的WOMAC®疗效参数的改善在六个月内得以维持。

结论

ART似乎是长期管理OA症状的一种安全有效的替代方法。

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