跳至主要内容
临床试验/NL-OMON41709
NL-OMON41709已完成不适用

A global comparison of Signature Guides and conventional instrumentation in the Oxford partial knee - GK7 Oxford Signature

BioMet0 个研究点目标入组 22 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
22

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

  • -Individuals with osteoarthritis or Avascular necrosis limited to the medial compartment of the knee that is also lacking patellofemoral or lateral compartment disease.
  • -Patients 21 and over.

排除标准

  • -Active Infection, sepsis or osteomyelitis
  • -Use of prosthesis in lateral compartment of the knee
  • -Rheumatoid arthritis or other forms of inflammatory joint disease
  • -Revision of failed prosthesis, failed upper tibial osteotomy, or post traumatic arthritis after tibial plateau fracture
  • -Insufficiency of the collateral, anterior, or posterior cruciate ligaments which would preclude stability of the device.
  • -Disease or damage to the lateral compartment of the knee
  • -Patients incapable of following directions regarding rehabilitation
  • -Patients who refuse, cannot, or should not receive a CT or MRI.

研究者

发起方
BioMet

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