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临床试验/NL-OMON52253
NL-OMON52253已完成不适用

MyLeg System: The functional evaluation of a powered knee-ankle prosthesis prototype for osseointegrated transfemural amputees - MyLeg System

Radboud Universitair Medisch Centrum0 个研究点目标入组 1 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1

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
18 至 99(—)

入选标准

  • 18 year or older and able to provide informed consent.
  • Underwent a uni-lateral transfemoral amputation and underwent a surgery
  • implementing the osseointegration
  • implant more than 2 years ago.
  • Able to walk independently (MFC-level K3 or higher)

排除标准

  • Vascular, neurological or musculoskeletal conditions or medication affecting
  • balance or gait
  • Patients with psychiatric disorders
  • Weight > 100 kg
  • Current problems with the alignment of the prosthesis
  • Fitted with a new prosthesis knee-component within the last 3 months or with a
  • new prosthesis ankle-component
  • within the last month

研究者

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