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临床试验/PACTR202009612835052
PACTR202009612835052Other未知

A Prospective Randomised Trial comparing Post-operative knee alignment following total knee replacement using patient specific knee instrumentation based on either CT or MRI.

Zimmer GmbH0 个研究点目标入组 70 人开始时间: 2020年9月4日最近更新:
适应症

试验速览

阶段
未知
状态
Other
发起方
Zimmer GmbH
入组人数
70

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
19 Year(s) 至 44 Year(s)(—)
性别
All

入选标准

  • 1.Patients suitable for primary Total Knee Replacement
  • 2.Patients with degenerative joint disease (inflammatory or non-inflammatory) or any of the composite diagnoses of:
  • a.Osteoarthritis
  • b.Avascular necrosis
  • c.Inflammatory Arthritis
  • d.Traumatic arthritis
  • 3.Patients aged over 18 and up to 80 years of age
  • 4.Patients with limited co-morbidity – ASA I – III
  • 5.Patients must be able to understand instructions and be willing to return for follow-up

排除标准

  • 1.Patients with significant co-morbidity - ASA IV - V
  • 2.Dementia and inability to understand and follow instructions
  • 3.Neurological conditions affecting moment
  • 4.Patients who are intolerant of placement in a CT or MRI gantry because of claustrophobia.

研究者

发起方
Zimmer GmbH

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