PAIN
Volume 146, Issue 3 , Pages 253-260, 5 December 2009

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

  • Amy S. Chappell

      Affiliations

    • Lilly Research Laboratories, Indianapolis, IN, USA
    • Corresponding Author InformationCorresponding author. Tel.: +1 317 277 3846; fax: +1 317 276 6026.
  • ,
  • Melissa J. Ossanna

      Affiliations

    • Lilly Research Laboratories, Indianapolis, IN, USA
  • ,
  • Hong Liu-Seifert

      Affiliations

    • Lilly Research Laboratories, Indianapolis, IN, USA
  • ,
  • Smriti Iyengar

      Affiliations

    • Lilly Research Laboratories, Indianapolis, IN, USA
  • ,
  • Vladimir Skljarevski

      Affiliations

    • Lilly Research Laboratories, Indianapolis, IN, USA
  • ,
  • Linda Chunhong Li

      Affiliations

    • i3 Statprobe, Ann Arbor, MI, USA
  • ,
  • Robert M. Bennett

      Affiliations

    • Oregon Health & Science University, Portland, OR, USA
  • ,
  • Harry Collins

      Affiliations

    • Anderson & Collins Clinical Research, Inc., Edison, NJ, USA

Received 11 June 2008; received in revised form 1 June 2009; accepted 18 June 2009. published online 22 July 2009.

Abstract 

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 (60–120mg/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 1 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 60–120mg/day, and 40.8% for placebo).

Keywords: Osteoarthritis, Pain, Duloxetine

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PII: S0304-3959(09)00369-8

doi:10.1016/j.pain.2009.06.024

PAIN
Volume 146, Issue 3 , Pages 253-260, 5 December 2009