Pfizer Global Research and Development, Groton, CT 06340, USA.
J Rheumatol. 2011 Dec;38(12):2643-52. doi: 10.3899/jrheum.110569. Epub 2011 Oct 1.
To evaluate the efficacy and safety of pregabalin monotherapy versus placebo for symptomatic pain relief and improvement of patient global assessment in patients with fibromyalgia (FM) enrolled from countries outside the United States.
This international, multicenter, double-blind, placebo-controlled trial randomly assigned 747 patients with FM to placebo or 300, 450, or 600 mg/day pregabalin twice daily for 14 weeks. Primary efficacy measures were endpoint mean pain scores and Patient Global Impression of Change (PGIC). Secondary outcomes included assessments of sleep and function.
Patients in the 450 mg/day pregabalin group showed significant improvements versus placebo in endpoint mean pain score (-0.56; p = 0.0132), PGIC (73% improved vs 56% placebo; p = 0.0017), and function [Fibromyalgia Impact Questionnaire (FIQ) total score -5.85; p = 0.0012]. PGIC was also significant for 600 mg/day pregabalin (69% improved; p = 0.0227). Results for these endpoints were nonsignificant for pregabalin at 300 mg/day and for pain and FIQ score at 600 mg/day. Early onset of pain relief was seen, with separation from placebo detected by Week 1 in all pregabalin groups. All pregabalin doses demonstrated superiority to placebo on the Medical Outcomes Study-Sleep Scale Sleep Disturbance subscale and the Sleep Quality diary. Dizziness and somnolence were the most frequently reported adverse events.
Pregabalin demonstrated modest efficacy in pain, global assessment, and function in FM at 450 mg/day, and improved sleep across all dose levels, but it did not provide consistent evidence of benefit at 300 and 600 mg/day in this study. Pregabalin was generally well tolerated for the treatment of FM. (Clinical trial registry NCT00333866).
评估普瑞巴林单药治疗与安慰剂相比在美国以外国家招募的纤维肌痛(FM)患者症状缓解和患者总体评估改善的疗效和安全性。
这项国际、多中心、双盲、安慰剂对照试验将 747 名 FM 患者随机分为安慰剂组或 300、450 或 600 mg/天普瑞巴林,每日两次,治疗 14 周。主要疗效指标为终点平均疼痛评分和患者总体印象变化(PGIC)。次要结局包括睡眠和功能评估。
与安慰剂相比,450mg/天普瑞巴林组患者在终点平均疼痛评分(-0.56;p=0.0132)、PGIC(73%改善,安慰剂为 56%;p=0.0017)和功能[纤维肌痛影响问卷(FIQ)总分-5.85;p=0.0012]方面均有显著改善。600mg/天普瑞巴林的 PGIC 也有显著改善(69%改善;p=0.0227)。普瑞巴林 300mg/天和 600mg/天的疼痛和 FIQ 评分的这些终点结果均无统计学意义。在所有普瑞巴林组中,从第 1 周开始即可观察到疼痛缓解的早期发作,并与安慰剂分离。所有普瑞巴林剂量在医疗结局研究-睡眠量表睡眠障碍亚量表和睡眠质量日记上均优于安慰剂。头晕和嗜睡是最常报告的不良事件。
在 450mg/天,普瑞巴林在疼痛、总体评估和功能方面显示出适度疗效,在所有剂量水平上改善睡眠,但在这项研究中,300 和 600mg/天并未提供一致的益处证据。普瑞巴林通常可耐受治疗纤维肌痛。(临床试验注册号 NCT00333866)。