跳至主要内容
临床试验/JPRN-jRCT1042220093
JPRN-jRCT1042220093招募中Unknown

Study of Efficacy of Spinal Cord DTM Stimulation via a Paddle-type Lead for Neuropathic Pain Following a Spinal Cord Lesion

Saito Ryuta0 个研究点目标入组 10 人开始时间: 2022年11月21日最近更新:
适应症

试验速览

阶段
Unknown
状态
招募中
发起方
入组人数
10

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 18age old 至 ot applicable(—)
性别
All

入选标准

  • Patients with intractable neuropathic pain following spinal cord lesion resistance to medication treatments
  • -18 years of age or older
  • -Pain scale of VAS (Visual analog scale) is more than 4 point
  • -Patients who classified as Frankel grade: B-E
  • -Patients in whom a paddle-shaped lead can be placed on the rostral side of the spinal cord lesion
  • -Patients who have obtained written consent from the patient

排除标准

  • -Patients for whom local and general anesthesia cannot be performed
  • -Patients who classified as Frankel grade A
  • -Patients receiving anti-cancer therapy
  • -Patients with a history of drug abuse
  • -Patients with high risk of surgery, such as patients with unstable angina pectoris and with end-stage liver disease presenting with hepatic encephalopathy
  • -Patients with diabetes mellitus who are not well controlled (HbA1c 9% or more)
  • -Patients with serious complications (liver disease, kidney disease, heart disease, lung disease, blood disease, brain disease, etc.)
  • -Pregnant or potentially pregnant patients
  • -Patients who are considered as inappropriate by a head of research or research assignations

研究者

发起方
Saito Ryuta

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