首页> 外文OA文献 >Imaging Pain Relief in Osteoarthritis (IPRO): protocol of a double-blind randomised controlled mechanistic study assessing pain relief and prediction of duloxetine treatment outcome
【2h】

Imaging Pain Relief in Osteoarthritis (IPRO): protocol of a double-blind randomised controlled mechanistic study assessing pain relief and prediction of duloxetine treatment outcome

机译:骨关节炎成像疼痛缓解(IPRO):一项评估疼痛缓解和度洛西汀治疗效果预测的双盲随机对照机制研究方案

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Introduction: Osteoarthritis (OA) pain is a major cause of long-term disability and chronic pain in the adult population. One in five patients does not receive satisfactory pain relief, which reflects the complexity of chronic pain and the current lack of understanding of mechanisms of chronic pain. Recently, duloxetine has demonstrated clinically relevant pain relief, but only in half of treated patients with OA. Here the aim is to investigate the neural mechanisms of pain relief and neural signatures that may predict treatment response to duloxetine in chronic knee OA pain.\udMethods and analysis: This is an ongoing single-centre randomised placebo-controlled mechanistic study (2:1 [placebo] allocation), using a multi-modal neuroimaging approach, together with psychophysiological [quantitative sensory testing], genetics and questionnaire assessments. Eighty-one subjects with chronic knee OA pain are planned to power for between group comparisons (placebo, duloxetine-responder, and duloxetine-non-responder). Participants have a baseline assessment and, following six weeks of duloxetine (30mg for two weeks, then 60mg for four weeks), a follow-up evaluation. Brain imaging is performed at 3T with blood-oxygen-level dependent functional magnetic resonance imaging at rest and during pin-prick nociceptive stimulation for main outcome assessment; arterial spin labelling and structural imaging (T1- weighted) for secondary outcome assessment. Questionnaires evaluate pain, negative affect, quality of sleep and cognition.\udEthics and dissemination: The study has been approved by the East Midlands – Nottingham 2 research ethics committee (18/EM/0189) and is being carried out under the principles of the Declaration of Helsinki (64th, 2013) and Good Clinical Practice standards. Results will be disseminated in peer-reviewed journals and at scientific conferences.
机译:简介:骨关节炎(OA)疼痛是成人人群长期残疾和慢性疼痛的主要原因。五分之一的患者无法获得令人满意的疼痛缓解,这反映出慢性疼痛的复杂性以及当前对慢性疼痛机制的了解不足。最近,度洛西汀已显示出与临床相关的疼痛缓解,但仅在一半的OA患者中得到了缓解。此处的目的是研究缓解疼痛的神经机制和神经信号,这些神经信号可能预测慢性膝OA疼痛对度洛西汀的治疗反应。\ ud方法与分析:这是一项正在进行的单中心随机安慰剂对照机制研究(2:1 [安慰剂]分配),使用多模态神经影像学方法,以及心理生理学[定量感觉测试],遗传学和问卷评估。计划对八十一名患有慢性膝OA疼痛的受试者进行组间比较(安慰剂,度洛西汀反应者和度洛西汀无反应者)。参与者进行了基线评估,并在度洛西汀治疗6周(30mg持续2周,然后60mg持续4周)后进行了随访评估。在3T时进行大脑成像,并在静止时和针刺伤害性刺激期间进行血氧水平依赖性功能磁共振成像,以评估主要结局。动脉自旋标记和结构成像(T1加权)以进行次要结果评估。问卷调查评估疼痛,​​负面影响,睡眠质量和认知质量。\ ud伦理与传播:该研究已由East Midlands – Nottingham 2研究伦理委员会(18 / EM / 0189)批准,并根据以下原则进行:赫尔辛基宣言(2013年第64号)和良好临床实践标准。结果将在同行评审的期刊和科学会议上发布。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号