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临床试验/NL-OMON46917
NL-OMON46917已完成不适用

Performance of MRK, NexGen and LCS <br>Total Knee Prosthesis based on AP Stability Measurement and PROMS<br> - Multicenter study AP-stability TKP

Antonius Ziekenhuis, Sneek0 个研究点目标入组 180 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
发起方
入组人数
180

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 knee replacement as determined jointly by the surgeon and the patient
  • * Over 18 years of age at time of surgery
  • * Patients who understand the conditions of the study and are willing to participate for the length of the prescribed term of follow-up.
  • * Patients who are capable of, and have given, informed consent to their participation in the study

排除标准

  • * Patients lacking capacity to or who will not provide consent
  • * Severe muscular, neurological or vascular deficiencies which compromise the affected extremity
  • * Bone deficiency or deficient bone quality likely to compromise the implant (as determined by surgical team on pre-operative radiographs)
  • * Severe ligament instability
  • * Hypersensitivity to the materials used
  • * Alcoholism or other addictive disorders
  • * Osteomyelitis
  • * Osteomalacia
  • * Severe Osteoporosis * clinical judgement
  • * Metabolic disorders which may impair bone formation
  • * Non correctable flexion contractures >20 degrees
  • * Varus/valgus deformities >15 degrees
  • * Those whose prospects for a recovery to independent mobility would be compromised by known pre-existing medical conditions

研究者

发起方
Antonius Ziekenhuis, Sneek

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