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临床试验/NCT00737581
NCT00737581已完成不适用

Posture Responsive Spinal Cord Stimulation Research Study

MedtronicNeuro2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2008年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
2

研究概览

简要总结

The purpose of this study is to characterize subjects' response to spinal cord stimulation with postural changes.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

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

  • Be ambulatory
  • Be 18 years of age or older
  • Have chronic low back pain and/or leg pain due to neuropathic causes
  • Be implanted with the Restore or Restore Advanced system for greater than or equal to 3 months
  • Be implanted with percutaneous thoracic leads
  • Have stable pain control
  • Adjust stimulation parameters manually on a regular basis
  • Be willing and able to complete protocol requirements
  • Be willing and able to provide written informed consent
  • Be male or nonpregnant female

排除标准

  • Plan to enroll in another clinical study during participation in this study, or currently enrolled in another clinical study
  • Be morbidly obese
  • Had pain-related surgery in the previous 12 weeks of enrollment or intend to undergo surgery during the period of the study

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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