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临床试验/NL-OMON28068
NL-OMON28068尚未招募不适用

The relation between pre-operative parameters and patient satisfaction after Total Knee Arthroplasty

Materialise N.V.0 个研究点目标入组 50 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
50

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

入选标准

  • Painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, or traumatic arthritis where one or more compartments are involved
  • Body-mass-index (BMI) below 35 kg/m2
  • High need to obtain pain relief and improve function
  • Ability and willingness to follow instructions, including control of weight and activity level, and to return for follow-up evaluations
  • Ability to work with a mobile device for tele-rehabilitation
  • Consent form read, understood and signed by patient

排除标准

  • Correction or revision of previous knee joint replacement procedure
  • Patients selected for a posterior stabilized implant type
  • Failure of previous joint replacement
  • Patients with severe pre-operative varus or valgus deformity greater than or equal to 15 degrees
  • BMI greater than or equal to 35 kg/m2
  • Not able or willing to undergo MRI and CT scan
  • Metal near knee joint (MRI-scan not possible)
  • Non-correctable varus axis
  • Uncooperative patient or patient with neurological disorders who is incapable of following directions

研究者

发起方
Materialise N.V.

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