跳至主要内容
临床试验/NCT02552095
NCT02552095已完成不适用

A Prospective, Single Arm, Multi Center Study on the Compatibility of Triathlon PKR and the Motion Analysis for Japanese

Stryker Japan K.K.10 个研究点 分布在 1 个国家目标入组 63 人开始时间: 2013年6月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
63
试验地点
10
主要终点
Change in Knee Injury and Osteoarthritis Outcome Score (KOOS)

研究概览

简要总结

The Purpose of this study is to evaluate compatibility of the Triathlon Partial Knee Replacement (PKR) with the Japanese population. It is expected that patients who receive the Triathlon PKR will achieve excellent clinical results without adverse effects and that the device fits well with Japanese morphology.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 79 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient requires a primary unicompartmental knee replacement.
  • Patient is between 20 years old to 80 years old.
  • Patient is diagnosed as osteoarthritis, rheumatoid arthritis, traumatic arthritis or avascular necrosis.
  • Patient can walk independently at least 10m.
  • Patient has signed the Institutional Review Board (IRB) approved, study specific informed patient consent form.
  • Patient is willing and able to comply with post-operative scheduled clinical and radiographic evaluations and rehabilitation.

排除标准

  • Patient requires a revision.
  • Patient is pregnant.
  • Patient has lateral osteoarthritis.
  • Patient has less than 10°of flexion contracture and greater than 90°of flexion.
  • Patient's preoperative mechanical alignment is less than 10° of varus and 15° of valgus.
  • Patient has had high tibial osteotomy, femoral osteotomy and/or joint fusion.
  • Patient has a neuromuscular or neurosensory deficiency that would limit the ability to assess the performance of the device.
  • Patient has a systemic or metabolic disorder leading to progressive bone deterioration.
  • Patient is immunologically suppressed or receiving steroids (>30 days) in excess of normal physiological requirements.
  • Patient has a deformity which will require the use of wedges or augments.
  • Patient has an active or suspected latent infection in or about the knee joint.
  • Patient who is inappropriate for participating in the study by the judgment of the investigator.

研究组 & 干预措施

Triathlon PKR

Other

Patient who receives the Triathlon.

干预措施: Triathlon PKR (Device)

结局指标

主要结局

Change in Knee Injury and Osteoarthritis Outcome Score (KOOS)

时间窗: Pre-operation, 6 months, 12 months and 24 months after surgery

次要结局

  • Change in Quality of life as assessed by 12-Item Short-Form Health Survey (SF-12) questionnaire(Pre-operation, 6 months, 12 months and 24 months after surgery)
  • Measurement of tibial resection plane (A-P length and width of resection)(intraoperative)
  • Change in Japanese Orthopaedics Association (JOA) score(Pre-operation, 6 months, 12 months and 24 months after surgery)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (10)

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