Duloxetine, a centrally acting analgesic, in the treatment of patients with osteoarthritis knee pain: A 13-week, randomized, placebo-controlled trial

被引:231
作者
Chappell, Amy S. [1 ]
Ossanna, Melissa J. [1 ]
Liu-Seifert, Hong [1 ]
Iyengar, Smriti [1 ]
Skljarevski, Vladimir [1 ]
Li, Linda Chunhong [2 ]
Bennett, Robert M. [3 ]
Collins, Harry [4 ]
机构
[1] Lilly Res Labs, Indianapolis, IN USA
[2] I3 Statprobe, Ann Arbor, MI USA
[3] Oregon Hlth & Sci Univ, Portland, OR 97201 USA
[4] Anderson & Collins Clin Res Inc, Edison, NJ USA
关键词
Osteoarthritis; Pain; Duloxetine; DOUBLE-BLIND; COMPARING DULOXETINE; REUPTAKE INHIBITOR; PHYSICAL SYMPTOMS; ARTHRITIS; DISABILITY; HYPERALGESIA; FIBROMYALGIA; MANAGEMENT; EFFICACY;
D O I
10.1016/j.pain.2009.06.024
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
Pain is a common cause of disability in osteoarthritis. Duloxetine, a serotonin and norepinephrine reuptake inhibitor (SNRI), has demonstrated analgesic effects in diabetic peripheral neuropathy and fibromyalgia. Considering its central mechanism of action, duloxetine may be effective in other pain states with evidence of central sensitization. Herein, we report the results of a 13-week, randomized, double-blind, placebo-controlled trial of duloxetine (60-120 mg/day) versus placebo in the treatment of knee pain in 231 patients meeting clinical and radiographic criteria for osteoarthritis of the knee. Duloxetine was Superior to placebo on the primary efficacy measure (weekly mean 24-h pain scores) beginning at Week I and continuing through the treatment period.(P <= .05). There was also a significant improvement in the WOMAC physical functioning subscale and several other secondary outcomes. Adverse-event rates did not differ significantly between treatment groups (49.5% for duloxetine 60-120 mg/day, and 40.8% for placebo). (C) 2009 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:253 / 260
页数:8
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