ACTRN12622000370707尚未招募未知
The enrolment of Total Hip (THA), Total Knee (TKA) or Partial Knee Arthroplasty (PKA) patients performed using either Stryker Mako Robotic-Arm Assisted Technology (Mako) or non-Mako techniques into an outcomes data registry.
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 500
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 21 Years 至 o limit（—）
- 性别
- All
入选标准
- •1. Patient has undergone or is to undergo a THA, TKA or PKA executed or to be executed via Mako or non-Mako techniques
- •2. Patient is a skeletally mature male or skeletally mature non-pregnant female aged 21 years or older at the time of consent
- •3. Patient has completed or is willing to complete the HREC-approved consent sign off via the myrecovery app
排除标准
- •1. Patient has a cognitive impairment, an intellectual disability or a mental illness that is thought by the Investigator to impact on their ability to comply with the requirements of the study
- •2. Patient is unwilling to complete the consent sign off via the myrecovery app
- •3. Patient has had revision/reconstruction of THA, TKA or PKA. Only primary surgeries will be included in this registry.
研究者
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