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临床试验/NCT06096155
NCT06096155已完成不适用

Ambispective Study to Assess the Safety and the Performance of SAGITTA EVL R Stem

Societe dEtude, de Recherche et de Fabrication2 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2023年6月13日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
46
试验地点
2
主要终点
Survival rate at mid/long term follow-up

研究概览

简要总结

This clinical study is conducted to collect data on hip arthroplasty with the SAGITTA EVL-R revision femoral stems manufactured by SERF.

This study will confirm the performance and safety of the SAGITTA EVL R revision femoral stems within the framework of MDR 2017/745 and in relation to the recommendations of the MEDDEV guide 2.7.1. Rev 4 (Clinical Evaluation Guide), which provides for a systematic procedure to monitor clinical data in order to verify the claimed performance of medical devices.

The primary objective is to evaluate the long-term survival rate (7 to 10 years post-op +/- 2 years) of SAGITTA EVL R stems.

Secondary objectives are to :

  • study long term patient satisfaction with their hip prosthesis,
  • confirm the long-term safety of these implants by studying the possible complications observed,
  • evaluate the performance of these implants using clinical scores.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient over 18 years old at the time of surgery,
  • Patient implanted with a SAGITTA EVL R revision femoral stem within its indications between 01/01/2010 and 31/12/2015,
  • Affiliated to French health insurance system

排除标准

  • Patient who has rejected to the use of his/her personal data,
  • Patient unable to understand the surgeon's instructions or to carry out the post-operative follow-up.

结局指标

主要结局

Survival rate at mid/long term follow-up

时间窗: At 7/10 years after surgery

Assess the survival rate at 7/10 year-follow-up, whatever the cause of revision

Survival Rate at Mid/Long Term Follow-up

时间窗: At 7/10 years after surgery

Assess the survival rate at 7/10 year-follow-up, whatever the cause of revision

次要结局

  • Oblivion of prosthesis(At 7/10 years after surgery)
  • Pain release(At 7/10 years after surgery)
  • Patient's satisfaction(At 7/10 years after surgery)
  • Adverse events(At 7/10 years after surgery)
  • Functional improvement(At 7/10 years after surgery)
  • Patient's Satisfaction(At 7/10 years after surgery)
  • Adverse Events(At 7/10 years after surgery)
  • Oblivion of Prosthesis(At 7/10 years after surgery)
  • Absence of Squeaking(At 7/10 years after surgery)
  • Functional Improvement(At 7/10 years after surgery)

研究者

发起方
Societe dEtude, de Recherche et de Fabrication
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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