单髁膝关节假体临床前体外测试方法探讨

      Test methods of pre-clinical evaluation of unicondylar knee prosthesis

      • 摘要: 相较于全膝关节置换,单髁置换具有最大限度地保留膝关节组织结构和运动功能的优点。临床前体外测试是评估单髁膝关节假体安全、有效的重要手段,同时也是监管上市时的重点关注项。该研究通过检索、对比、分析现行法规、技术标准、指导原则和相关研究文献,阐述单髁膝关节假体临床前体外测试的相关研究方法,同时结合现行审评要求及审评经验对单髁膝关节假体产品注册审评过程中的临床前性能研究关注点进行探讨,通过进一步明晰该类产品的性能评价要求,以期为单髁膝关节假体的临床前性能研究以及规范行业测试标准提供借鉴思路。

         

        Abstract: Compared with total knee arthroplasty, unicondylar replacement has the advantage of preserving the knee tissue structure and motor function to the greatest extent. Pre-clinical in-vitro test is an important tool to evaluate the safety and effectiveness of unicondylar knee prostheses, and it is also a key focus of the product registration process. Through the collection, comparison, and analysis of current regulations, technical standards, guidelines, and related research literature, this paper expounds on the relevant research methods for the pre-clinical in vitro testing of unicondylar knee prostheses. At the same time, in conjunction with current evaluation requirements and experience, the study discusses the focus of pre-clinical performance research for unicondylar knee prostheses during the registration process to clarify the performance evaluation requirements of this product. This aims to provide a reference for the pre-clinical performance research of unicondylar knee prostheses and to standardize industry testing standards.

         

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