DRKS00023167暂停不适用
Clinical testing of a new, CE-certified joint mechanism (MUTARS® HD coupling C-O-M) for the implantation of a tumour or revision prosthesis in the area of the knee joint - MUTARS HD C-O-M
niversitätsklinikum Essen0 个研究点目标入组 175 人开始时间: 2020年10月19日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 暂停
- 发起方
- 入组人数
- 175
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
- one 至 one（—）
- 性别
- All
入选标准
- •1. Patients for which a tumour prosthesis of the proximal tibia or the type MUTARS® total knee, as well as MUTARS® distal femur, needs to be implanted. Indication for tumorresection and reconstruction is also given within the sarcoma-tumor-conference.
- •1.Patients are included for which a replacement operation to a revision endoprosthesis type GenuX® MK or KRI or instead to the systems MUTARS® proximal tibia or MUTARS® femur is necessary due to failure (e.g. infection, loosening, perioperative fracture) of a previously implanted knee endoprosthesis.
排除标准
- •Patients without any indication for implantation of tumor prosthesis (decision of tumor conference) in case of sarcoma or metastasis. Furthermore excluded are patients without any need to implant an axis-guided prosthesis in case of revision surgery.
研究者
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