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临床试验/NCT06644807
NCT06644807招募中不适用

Neuromodulation Methods for Suppressing Phantom Limb Pain

Skolkovo Institute of Science and Technology2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2024年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
50
试验地点
2
主要终点
Visual analogue scale (VAS)

研究概览

简要总结

This study assesses the effectiveness of neuromodulation in alleviating pain through the stimulation of peripheral nerves. The research involves implanting electrodes for test stimulation of peripheral nerves (PNS - Peripheral Nerve Stimulation), spinal cord (SCS - Spinal Cord Stimulation), dorsal root ganglia (DRGS - Dorsal Root Ganglion Stimulation), and motor cortex (MCS - Motor Cortex Stimulation). The study aims to explore the use of neuromodulation for pain relief in patients experiencing pain due to upper or lower limb amputation.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Amputation of the upper limb at the level of the forearm or upper arm, or amputation of the lower limb at the level of the lower leg or thigh.
  • Age between 18 and 65 years.
  • Duration since amputation is at least 6 months.
  • Presence of persistent chronic pain syndrome rated between 4 and 10 on the Visual Analog Scale (VAS).
  • Absence of pregnancy at the time of implantation, confirmed by a pregnancy test (for female participants only).
  • Signed consent to participate in the study.

排除标准

  • Presence of severe somatic pathology that hinders surgical treatment and participation in the study.
  • Presence of psychiatric disorders (including a history of), severe depression, suicidal tendencies, or a history of suicide attempts.
  • Presence of severe orthopedic deformity in the limb above the level of amputation.
  • History of cancer.
  • History of epilepsy.
  • Complicated traumatic brain injury (TBI) or a history of stroke.
  • Inability to undergo electrostimulation due to other somatic pathology.
  • Purulent-septic pathology.
  • Drug addiction (including a history of).
  • Congenital anomaly of upper limb development.
  • Anomalies in the development of the central and peripheral nervous systems.

结局指标

主要结局

Visual analogue scale (VAS)

时间窗: Up to 4 months

The Visual Analog Scale (VAS) is a 10 cm line used to measure pain intensity. One end of the line represents \"no pain,\" while the other end signifies \"worst possible pain.\" The line can be either horizontal or vertical.

SF-36

时间窗: up to 1 year

The questionnaire consists of 36 items grouped into eight scales: physical functioning, role limitations due to physical health, bodily pain, general health, vitality, social functioning, emotional well-being, and mental health. Each scale ranges from 0 to 100, where 100 represents full health. Higher scores indicate better quality of life, with two summary measures: physical and mental well-being.

次要结局

  • Sensory mapping(up to 4 months)
  • Pain detect(Up 1 year)
  • DN 4(up to 1 year)
  • Hospital Anxiety and Depression Scale, HADS(up to 1 year)
  • Sensory threshold(up to 6 months)

研究者

发起方
Skolkovo Institute of Science and Technology
申办方类型
Other
责任方
Sponsor

研究点 (2)

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