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临床试验/NCT02051959
NCT02051959暂停不适用

Long-Term Treatment of Patients Experiencing Phantom Limb Pain With Transcranial Direct Current Stimulation (tDCS)

Sheba Medical Center1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2015年5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
暂停
入组人数
24
试验地点
1
主要终点
Reduced phantom limb pain

研究概览

简要总结

  • Phantom limb pain (PLP) refers to pain in a limb that has been amputated or deafferented. Phantom limb pain might be related to brain cortical plastic changes.
  • The purpose of this study is to determine the efficacy of a series of transcranial direct current stimulation (tDCS) sessions, a non-invasive and focal brain stimulation method, in producing long-term reduction of phantom limb pain among amputees who experience such pain.

This is a Crossover sham control.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age 18 to 80
  • •Limb amputation from at least 6 months before study enrollment
  • •Presence of PLP at least 2 times a week and present 4 weeks prior to onset of study
  • •Written informed consent

排除标准

  • •Coexistence of major neurological or psychiatric diseases
  • •Being actively enrolled in a separate study targeting pain relief
  • •Post traumatic stress disorder (PTSD) diagnosed patients
  • •Any contraindication to noninvasive brain stimulation such as past brain surgery, brain implants, cochlear implant, epilepsy or any past seizure
  • •Pregnant women
  • •Within the traumatic amputees group - subjects diagnosed with diabetes

研究组 & 干预措施

Crossover 1a: anodal stimulation of M1 + sham

Active Comparator

6 amputees will undergo 8 active treatments of 20 min 2mA anodal stimulation of M1 localized to the contralateral amputation area followed by 8 sham treatments.

Total duration and frequency of treatments: 8 weeks, 2 sessions per week.

Each session will last approximately one hour which will consist of:

  • EEG and pain measurements
  • 20 minutes of stimulation
  • EEG and pain measurements after completion of stimulation

干预措施: Anodal stimulation of M1 + sham (Device)

Crossover 1b: sham + anodal stimulation of M1

Active Comparator

6 amputees will undergo 8 sham treatments followed by 8 active treatments of 20 min 2mA anodal stimulation of M1 localized to the contralateral amputation area.

Total duration and frequency of treatments: 8 weeks, 2 sessions per week.

Each session will last approximately one hour which will consist of:

  • EEG and pain measurements
  • 20 minutes of stimulation
  • EEG and pain measurements after completion of stimulation

干预措施: Sham + Anodal stimulation of M1 (Device)

Crossover 2a: cathodal stimulation of M1 + sham

Active Comparator

6 amputees will undergo 8 active treatments of 20 min 2mA cathodal stimulation of M1 localized to the contralateral amputation area followed by 8 sham treatments.

Total duration and frequency of treatments: 8 weeks, 2 sessions per week.

Each session will last approximately one hour which will consist of:

  • EEG and pain measurements
  • 20 minutes of stimulation
  • EEG and pain measurements after completion of stimulation

干预措施: Cathodal stimulation of M1 + sham (Device)

Crossover 2b: sham + cathodal stimulation of M1

Active Comparator

6 amputees will undergo 8 sham treatments followed by 8 active treatments of 20 min 2mA cathodal stimulation of M1 localized to the contralateral amputation area.

Total duration and frequency of treatments: 8 weeks, 2 sessions per week.

Each session will last approximately one hour which will consist of:

  • EEG and pain measurements
  • 20 minutes of stimulation
  • EEG and pain measurements after completion of stimulation

干预措施: Sham + Cathodal stimulation of M1 (Device)

结局指标

主要结局

Reduced phantom limb pain

时间窗: 5 months after last stimulation session

Reduction of phantom limb pain compared to phantom limb pain before treatment, according to Visual Analog Scales (VAS) evaluation

次要结局

  • Adverse effects of treatment(Up to 5 weeks)
  • Effects of treatment on the electrical activity of the brain(Up to 5 weeks)

研究者

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

Dr. Itzhak Siev-Ner

Head of The Department of Orthopedic Rehabilitation

Sheba Medical Center

研究点 (1)

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