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A randomized, double-blind, multicenter, placebo-controlled phase III trial to evaluate the efficacy and safety of pregabalin in Japanese patients with fibromyalgia

机译:一项随机,双盲,多中心,安慰剂对照的III期临床试验,评估普瑞巴林在日本纤维肌痛患者中的疗效和安全性

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Introduction: Fibromyalgia is a chronic disorder characterized by widespread pain and tenderness. Prior trials have demonstrated the efficacy of pregabalin for the relief of fibromyalgia symptoms, and it is approved for the treatment of fibromyalgia in the United States. However, prior to this study, there has not been a large-scale efficacy trial in patients with fibromyalgia in Japan.Methods: This randomized, double-blind, multicenter, placebo-controlled trial was conducted at 44 centers in Japan to assess the efficacy and safety of pregabalin for the symptomatic relief of pain in fibromyalgia patients. Patients aged ≥18 years who had met the criteria for fibromyalgia were randomized to receive either pregabalin, starting at 150 mg/day and increasing to a maintenance dose of 300 or 450 mg/day, or placebo, for 15 weeks. The primary efficacy endpoint was mean pain score at final assessment. Secondary endpoints included Patient Global Impression of Change (PGIC) together with measures of sleep, physical functioning and quality of life.Results: A total of 498 patients (89% female) were randomized to receive either pregabalin (n = 250) or placebo (n = 248). Pregabalin significantly reduced mean pain score at final assessment (difference in mean change from baseline, compared with placebo -0.44; P = 0.0046) and at every week during the study (P <0.025). Key secondary endpoints were also significantly improved with pregabalin treatment compared with placebo, including PGIC (percentage reporting symptoms "very much improved" or "much improved", 38.6% vs 26.7% with placebo; P = 0.0078); pain visual analog scale (difference in mean change from baseline, compared with placebo -6.19; P = 0.0013); Fibromyalgia Impact Questionnaire total score (-3.33; P = 0.0144); and quality of sleep score (-0.73; P <0.0001). Treatment was generally well tolerated, with somnolence and dizziness the most frequently reported adverse events.Conclusions: This trial demonstrated that pregabalin, at doses of up to 450 mg/day, was effective for the symptomatic relief of pain in Japanese patients with fibromyalgia. Pregabalin also improved measures of sleep and functioning and was well tolerated. These data indicate that pregabalin is an effective treatment option for the relief of pain and sleep problems in Japanese patients with fibromyalgia.Trial Registration: ClinicalTrials.gov: NCT00830167.
机译:简介:纤维肌痛是一种以广泛的疼痛和压痛为特征的慢性疾病。先前的试验已经证明了普瑞巴林减轻纤维肌痛症状的功效,并且在美国已被批准用于治疗纤维肌痛。然而,在此研究之前,日本尚无针对纤维肌痛患者的大规模疗效试验。方法:这项随机,双盲,多中心,安慰剂对照试验在日本的44个中心进行,以评估疗效普瑞巴林在缓解纤维肌痛患者疼痛中的作用和安全性。 ≥18岁且符合纤维肌痛标准的患者被随机分配接受普瑞巴林治疗,剂量从150 mg /天开始,并增加至300或450 mg /天的维持剂量,或安慰剂治疗15周。主要功效终点为最终评估时的平均疼痛评分。次要终点包括患者的整体变化印象(PGIC)以及睡眠,身体功能和生活质量的测量结果。结果:总共498例患者(89%为女性)被随机分配接受普瑞巴林(n = 250)或安慰剂( n = 248)。普瑞巴林显着降低了最终评估时的平均疼痛评分(与安慰剂相比,基线平均改变差异-0.44; P = 0.0046)以及研究期间的每周(P <0.025)。与安慰剂相比,普瑞巴林治疗的主要次要终点也显着改善,包括PGIC(报告症状“大大改善”或“大大改善”的百分比,分别为38.6%和26.7%,安慰剂)(P = 0.0078);疼痛视觉模拟量表(与安慰剂相比,与基线的平均变化差异为-6.19; P = 0.0013);纤维肌痛影响问卷总评分(-3.33; P = 0.0144);和睡眠质量得分(-0.73; P <0.0001)。结论:该研究证明普瑞巴林的剂量高达450 mg / day,对于症状缓解的日本纤维肌痛患者而言是有效的,治疗通常耐受良好,其中嗜睡和头晕是最常见的不良事件。普瑞巴林还改善了睡眠和功能指标,并且耐受性良好。这些数据表明,普瑞巴林是缓解日本纤维肌痛患者疼痛和睡眠问题的有效治疗选择。试验注册:ClinicalTrials.gov:NCT00830167。

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