跳至主要内容
临床试验/NCT00460161
NCT00460161暂停3 期

Acupuncture for Phantom Limb Pain: A Randomized, Double-Blind, Placebo/Sham - Controlled Study

Shaare Zedek Medical Center2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2009年2月最近更新:
适应症

试验速览

阶段
3 期
状态
暂停
入组人数
40
试验地点
2
主要终点
To study the effect of acupuncture on phantom limb pain at 4 weeks post-amputation

研究概览

简要总结

Phantom pain is a common complication following limb amputation, and is thought to result from a system of pathophysiological mechanisms - peripheral, spinal, central and psychological. Treatment is primarily medical, using antidepressant and anticonvulsant medications. At present, there is no evidence-based approach for the management of phantom limb pain (PLP). Acupuncture is an ancient Chinese treatment during which thin needles (diameter 0.20-0.30mm) are inserted into various points on the skin. Studies of this treatment have found significant benefit in a number of conditions with chronic pain.

We propose a randomized, double-blind, placebo/sham -controlled study to evaluate whether acupuncture is an effective and safe modality for preventing and reducing PLP in patients following lower limb amputation. Patients requiring lower limb amputation (above-ankle) will be randomized into two groups, for real or placebo/sham acupuncture treatment. Both groups will be treated twice-weekly with a standardized (as opposed to individualized) acupuncture treatment protocol, using either true or placebo needles at sham acupuncture points, for a period of four weeks (eight treatments).

The primary outcome to be evaluated will be PLP at 4 weeks, using a site-specific numerical rating pain scale (ss-NRS). Secondary outcome measures to be evaluated are: stump pain (ss-NRS); analgesic use (Tramadol, 100mg Tablet); and depressive symptoms, using the Beck Depression Score. Blinding of the participants will be evaluated using a Validation of Blinding Questionnaire at the end of the treatment period.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients of either gender
  • Age 18 years and older
  • Scheduled for lower single limb amputation (above or below knee)
  • Ability to comply with study protocol

排除标准

  • Patients requiring limb amputation due to trauma
  • Patients displaying symptoms of overt Axis-1 psychopathology such as Schizophrenia or Substance Abuse
  • Inability to comply with the study protocol
  • Previous experience with acupuncture treatment; current use of complementary or alternative medical treatments.

结局指标

主要结局

To study the effect of acupuncture on phantom limb pain at 4 weeks post-amputation

时间窗: 4 weeks

次要结局

  • To study the effect of acupuncture on phantom limb pain at 3 months post-amputation(3 months)
  • To study the effect of acupuncture on stump pain at 4 weeks post-amputation(4 weeks)
  • To study the effect of acupuncture on parameters of depression (using the Beck Depression Score) at 4 weeks and 3 months post-amputation(4 weeks and 3 months)
  • To study the safety of acupuncture treatment in patients following amputation with phantom limb pain(4 weeks)
  • To study the effect of acupuncture on analgesic use (Tramadol 100mg) during the first 4 weeks post-amputation(4 weeks)

研究者

申办方类型
Other

研究点 (2)

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