跳至主要内容
临床试验/NL-OMON50362
NL-OMON50362已完成4 期

A CLINICAL RANDOMIZED CONTROLLED RSA TRIAL COMPARING THE CEMENTLESS ATTUNE ROTATING PLATFORM KNEE SYSTEM TO THE CEMENTLESS LCS ROTATING PLATFORM KNEE SYSTEM - RSA RCT: ATTUNE RP TKA versus LCS RP TKA

Spaarne Ziekenhuis0 个研究点目标入组 61 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
61

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

  • Age: 21- 90 years Indications: Patient is diagnosed with osteoarthritis and
  • requiring primary knee arthroplasty General: All consecutive patients
  • (*usual care*) are included to prevent selection bias in the
  • migration analysis. Consent: Patient is capable of giving informed consent
  • and expressing a willingness to comply

排除标准

  • The patient has an a-priori risk for a posterior-stabilized total knee
  • arthroplasty.
  • - Status after patellectomy
  • - In case flexion is less than 90 degrees The patient is unable or unwilling to
  • sign the Informed Consent specific to this study The patient does not
  • understand the Dutch or English language good enough to participate Patients
  • indicated for revision arthroplasty Patient is diagnosed with rheumatoid
  • arthritis When there are not enough markers visible in the baseline RSA
  • photograph and it will not improve by
  • placing the patient in another position, the patient will be
  • excluded from the study (secondary

研究者

发起方
Spaarne Ziekenhuis

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