跳至主要内容
临床试验/NCT02070016
NCT02070016撤回不适用

Clinical Applicaitons of Non-Invasive Brain Stimulation for the Treatment of Chronic Pain

Stanford University1 个研究点 分布在 1 个国家开始时间: 2014年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Change in Average Daily Pain

研究概览

简要总结

The purpose of this study is to test whether non-invasive brain stimulation, such as Transcranial Magnetic Stimulation (TMS) may alleviate pain associated with various chronic pain conditions. We will test various methods of TMS to identify a treatment approach that may reduce the symptoms of chronic pain for the patient.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Participant)

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

  • Age 18 or older
  • Patient with Chronic Low Back Pain
  • Meets minimum pain level criteria
  • Ability to perform the experimental Task and Procedures

排除标准

  • MRI contraindication if an MRI exam is required per protocol
  • TMS Contraindication
  • History of a psychological or psychiatric disorder that would interfere with study procedures, at the discretion of the researcher.
  • Neurologic illness that would interfere with brain integrity
  • Current medical condition or medication use that would interfere with study procedures or data integrity, at the discretion of the researcher.
  • Currently pregnant or planning to become pregnant.
  • On going legal action or disability claim.

研究组 & 干预措施

TMS Parameter Condition 1 first

Experimental

Application of Transcranial Magnetic Stimulation

干预措施: Transcranial Magnetic Stimulation (Device)

TMS Parameter Condition 2 First

Experimental

Application of Transcranial Magnetic Stimulation

干预措施: Transcranial Magnetic Stimulation (Device)

结局指标

主要结局

Change in Average Daily Pain

时间窗: Baseline Compared to each treatmeant series (at 4 weeks, 8 weeks, and 12 weeks)

Compared to baseline pain report as provided by Visual Analogue Scale (VAS)

Change in Worst Daily Pain

时间窗: Baseline Compared to each treatment series (at 4 weeks, 8 weeks, and 12 weeks)

As compared to baseline worst daily pain report provided on visual analogue scale (VAS)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sean Mackey

Chief, Division of Pain Medicine

Stanford University

研究点 (1)

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