跳至主要内容
临床试验/NL-OMON52619
NL-OMON52619招募中不适用

Construct stability with the use of cones in revision total knee arthroplasty measured with RSA - Cones RSA

Sint Maartenskliniek0 个研究点目标入组 25 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
招募中
入组人数
25

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 64(—)

入选标准

  • Patients requiring a (re-(re-))revision of their total knee arthroplasty and
  • the Legion system with the use of a cone in the tibia because of metaphyseal
  • Patient is willing to consent to participate in the study.
  • Patient is <78 years old
  • Patient plans to be available for follow-up through five years post-operative.
  • Patient is in stable health and is free of or treated and stabilized for
  • cardiac, pulmonary, haematological, or other conditions that would pose
  • excessive operative risk ( < ASA II).

排除标准

  • Indication for a hinged-type revision system.
  • Active, local infection or systemic infection.
  • Patient has physical, emotional, or neurological conditions that would
  • compromise the patient*s compliance with postoperative rehabilitation and
  • follow-up.
  • Patient has an immunosuppressive disorder (including inflammatory arthritis).
  • Patient has a known sensitivity to materials in the device.

研究者

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