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临床试验/ACTRN12611001071910
ACTRN12611001071910已完成未知

TriathlonPA-11 - A retrospective review of Safety and Efficacy of Stryker Triathlon cementless components with Peri-Apatite in Total Knee Replacement

Stryker Australia Pty Ltd0 个研究点目标入组 100 人开始时间: 2011年10月14日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
100

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

年龄范围
o limit 至 o limit(—)
性别
All

入选标准

  • •1. The patient received a primary cementless Triathlon Total Knee with Peri-Apatite which was performed by Dr Dermot Collopy and is a minimum of 2 years post-surgery.
  • •2. The patient has signed the study specific, HREC-approved, Informed Consent document.
  • •3. The patient is willing and able to comply with the specified clinical and radiographic evaluations.

排除标准

  • •1. Patient has a cognitive impairment, an intellectual disability or a mental illness 2. Patients who received a Triathlon PS Femoral Cementless Component 3. Pregnant Women

研究者

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