...
首页> 外文期刊>The journal of pain: official journal of the American Pain Society >Treatment of chronic low back pain with etoricoxib, a new cyclo-oxygenase-2 selective inhibitor: improvement in pain and disability--a randomized, placebo-controlled, 3-month trial.
【24h】

Treatment of chronic low back pain with etoricoxib, a new cyclo-oxygenase-2 selective inhibitor: improvement in pain and disability--a randomized, placebo-controlled, 3-month trial.

机译:使用一种新的环加氧酶2选择性抑制剂依托考昔治疗慢性下背痛:疼痛和残疾的改善-一项随机,安慰剂对照,为期3个月的试验。

获取原文
获取原文并翻译 | 示例
           

摘要

We evaluated etoricoxib, a novel COX-2-specific inhibitor, in 319 patients with chronic low back pain (LBP) in this double-blind, placebo-controlled trial. Patients were randomized to a 60 mg dose (n = 103) or 90 mg dose (n = 107) of etoricoxib, or placebo (n = 109), daily for 12 weeks. The primary endpoint was low back pain intensity scale (Visual Analog Scale of 0- to 100-mm) time-weighted average change from baseline over 4 weeks. Other endpoints included evaluation over 3 months of low back pain intensity scale, Roland-Morris Disability Questionnaire (RMDQ), low back pain bothersomeness scale, patient- and investigator-global assessments, Patient Health Survey (MOS SF-12), rescue acetaminophen use, and discontinuation due to lack of efficacy. Etoricoxib provided significant improvement from baseline versus placebo in pain intensity (4 weeks: 12.9 mm and 10.3 mm for 60-mg and 90-mg doses, P <.001 for each; 12 weeks: 10.5 mm and 7.5 mm for 60-mg and 90-mg doses, P =.001 and.018, respectively). Etoricoxib at either dose led to significant improvement in other endpoints, including RMDQ scores, bothersomeness scores and global assessments. Etoricoxib given once daily provided significant relief of symptoms, and disability associated with chronic LBP that was observed 1 week after initiating therapy, was maximal at 4 weeks, and was maintained over 3 months.
机译:在这项双盲,安慰剂对照试验中,我们评估了319种慢性下腰痛(LBP)患者中的新型COX-2特异性抑制剂依托考昔。每天将患者随机分为60 mg剂量(n = 103)或90 mg剂量(n = 107)的依托昔布或安慰剂(n = 109),持续12周。主要终点是4周内从基线开始的时间加权平均腰背痛强度量表(视觉模拟量表为0至100mm)。其他终点包括3个月内的下背痛强度量表评估,Roland-Morris残疾问卷(RMDQ),下背痛困扰量表,患者和研究者全球评估,患者健康调查(MOS SF-12),对乙酰氨基酚的紧急使用,以及由于缺乏疗效而停药。与安慰剂相比,Etoricoxib的疼痛强度有显着改善(4周:60 mg和90 mg剂量分别为12.9 mm和10.3 mm,每个P <.001; 12周:60 mg和1mg为10.5 mm和7.5 mm) 90毫克剂量,分别为P = 0.001和.018)。两种剂量的依托昔布都导致其他终点的显着改善,包括RMDQ评分,打扰度评分和整体评估。每天一次给予埃托昔布可显着缓解症状,在开始治疗后1周观察到与慢性LBP相关的残疾,在4周时最大,并维持3个月以上。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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