跳至主要内容
临床试验/DRKS00013785
DRKS00013785招募中未知

Pilot study on feasibility and usability of the brain-computer interface-controlledMoreGrasp neuroprosthesis for individuals withcervical spinal cord injury - MoreGrasp

niversitätsklinikum Heidelberg - Klinik für Paraplegiologie - Experimentelle Neurorehabilitation0 个研究点目标入组 15 人开始时间: 2018年1月22日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
15

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
N/a: Single Arm Study
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • Sub-acute to chronic cervical SCI with time since injury = 6 months and missing or weak grasp function
  • - Age over 17
  • - Sufficient voluntary shoulder movements and elbow flexion on one side, preferably on the dominant side
  • - Capacity to consent

排除标准

  • - Severe restrictions in the passive range of movement of the joints of the upper limb (> 30% of physiological range of motion)
  • - Severe spasticity in the upper limbs
  • - Skin diseases like infections, psoriasis, burns etc. at the upper limbs
  • - Hyperesthesia of the upper limbs (upper and lower arm), which would not allow to increase FES intensity to a sufficient level of contraction force
  • - Cardiac pacemaker, other active implants like medication pumps, phrenic pacemaker etc.
  • - Metal implants in the direct area of current flow under the stimulation electrodes
  • - Plexus paresis or other injuries / diseases that lead to extensive denervation of muscles of the upper limbs
  • - Known history of epilepsy
  • - Severe cognitive impairment or psychiatric conditions that restrict the use of a neuroprosthesis
  • - Pregnancy

研究者

发起方
niversitätsklinikum Heidelberg - Klinik für Paraplegiologie - Experimentelle Neurorehabilitation

相似试验