跳至主要内容
临床试验/NL-OMON54033
NL-OMON54033尚未招募不适用

Migration of the Restoris MultiCompartmental Knee Implant System in robotic-assisted unicompartmental knee arthroplasty: a 5 year follow up RSA study - RSA Restoris MCK study

Reinier Haga Orthopedisch Centrum0 个研究点目标入组 33 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
尚未招募
发起方
入组人数
33

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 至 99(—)

入选标准

  • - Indication for medial unicompartmental knee replacement mainly as a result of
  • moderately disabling joint disease because of: Painful osteo- or post-traumatic
  • arthitis or as an alternative to tibial osteotomy. - Patient qualified for UKP
  • based on physical exam and medical history - Patient is able to speak and write
  • Dutch - Patient is willing to participate and able to provide written informed
  • consent - Age > 18 years

排除标准

  • - contraindication as described by the manufacturer
  • - patient has a known or suspected sensitivity or allergy to one or more
  • of the implant materials
  • - revision UKP surgery of the same compartment

研究者

发起方
Reinier Haga Orthopedisch Centrum

相似试验

Migration of the Restoris MultiCompartmental Knee... | 临床试验