跳至主要内容
临床试验/DRKS00006779
DRKS00006779已完成不适用

Evaluation of clinical, neurophysiological and imaging parameter to detect and characterize chronic central neuropathic pain after spinal cord injury

Klinik für Paraplegiologie,Universitätsklinikum Heidelberg0 个研究点目标入组 27 人开始时间: 2014年9月23日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
27

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 65 Years(—)
性别
All

入选标准

  • Able to consent; chronic spinal cord injury at least 12 months post injury; neurological Level of injury C5 to Th10

排除标准

  • Sensory impairment in dermatome C2 on both sides; artificial respiration; cauda-equina syndrome; epilepsy; impaired cognitive ablilities; pre-existing mental disorder; cardiac pacemaker; other active implants (e.g. phrenic pacemaker, drug pumps); metal implants less than 20 cm away from electrodes for electrical stimulation; severe traumatic brain injury in clinical history; pre-existing sensory deficits or dieseases which entail polyneuropathy (e.g. diabetes mellitus); severe primary internistic diseases (e.g. oncological, cardilogical); pregnancy.

研究者

发起方
Klinik für Paraplegiologie,Universitätsklinikum Heidelberg

相似试验