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临床试验/ACTRN12611000289910
ACTRN12611000289910招募中不适用

A multicentre, prospective, consecutive clinical study of the anthropometric dimensions of the Genesis II and Genesis II Slim Total Knee Prostheses in patients with degenerative joint disease requiring knee replacement.

Smith & Nephew0 个研究点目标入组 1,060 人开始时间: 2011年3月18日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
1,060

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
Non-randomised trial
主要目的
Treatment

入排标准

年龄范围
o limit 至 80 Years(—)
性别
All

入选标准

  • Patient presents with non-inflammatory degenerative joint disease of predominantly the medial compartment requiring knee replacement.
  • Patient, or his/her legal guardian, has given consent to participate in the study.
  • Patient plans to be available for follow-up through to 2 years postoperative.

排除标准

  • Patient is known to have insufficient femoral or tibial bone stock.
  • Patient is immunosuppressed or has an autoimmune disorder.
  • Patient has inflammatory arthritis (e.g. rheumatoid arthritis).
  • Patient has had major, non-arthroscopic surgery to the study knee.
  • Patient has an active, local infection or systemic infection.
  • Patient has a physical, emotional or neurological condition that would compromise compliance with postoperative rehabilitation and follow-up.
  • Patient has hip arthritis and/or replacement.
  • Patient has lateral knee compartment disease (e.g. valgus knee).
  • Patient is pregnant or plans to become pregnant during the course of the study.
  • Patient is on workman’s compensation.
  • Serious medical infirmity (e.g. Parkinson’s disease, Alzheimer’s disease, CVA with neurological deficit)
  • Symptomatic spinal disease.
  • Age over 80 years.

研究者

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