ROSA Total Knee Post Market Study EMEA
| 适应症 | Knee Pain, Chronic Osteoarthritis, Avascular Necrosis of the Femoral Condyle, Moderate Varus, Valgus or Flexion Deformities |
|---|---|
| 分期 | 不适用 |
| 申办方 | Zimmer Biomet |
| 状态 | 已完成 |
| 受试者人数 | 252 人 |
| 干预（药物） | Device: Persona Total Knee, Device: NexGen Total Knee, Device: Vanguard Total Knee |
| 开始日期 | 2020年12月15日 |
| 完成日期 | 2025年8月22日 |
| 结果公布日 | 2026年1月21日 |
摘要
This is a prospective, multicenter clinical study designed to facilitate the collection and evaluation of surgical workflow efficiency, patient pain and function outcome and adverse events data. This study might include Persona, Nexgen and Vanguard product families using the ROSA Total Knee Robotic system or conventional instrumentation. The primary objective is to evaluate the accuracy of implant alignment for ROSA Total Knee robotic instrumentation compared to conventional instrumentation.
Alignment Accuracy
在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文
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