跳至主要内容
临床试验/NCT05003414
NCT05003414进行中(未招募)不适用

A Prospective, Multicentre, International, Post-marketing, Longitudinal, Observational Cohort Study to Monitor the Performances of GMK Sphere Cementless Knee Prosthesis

Medacta International SA5 个研究点 分布在 2 个国家目标入组 200 人开始时间: 2020年1月14日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
200
试验地点
5
主要终点
Survival rate

研究概览

简要总结

This is a Post-Marketing Surveillance study of GMK Sphere cementless knee prosthesis.

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 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • A disabled or severely disabled joint as a result of arthritis, traumatic arthritis, rheumatoid arthritis, poly-arthritis or avascular necrosis
  • Patients between the age of 18 and 80 at the time of consent
  • Listed for total knee replacement surgery.
  • Patients who are willing and able to give informed written consent

排除标准

  • Progressive local or systemic infection
  • Muscular loss, neuromuscular disease or vascular deficiency of the affected limb, making the operation unjustifiable
  • Severe instability secondary to advance destruction of condralar structures or loss of integrity of the medial or lateral ligament
  • Those whose prospects for a recovery to independent mobility would be compromised by known coexistent, medical problems
  • Patient whose BMI exceeds 40
  • Any case not described in the inclusion criteria

结局指标

主要结局

Survival rate

时间窗: 10 years

Kaplan Meier method

次要结局

  • Clinical outcome: Knee Society score(Preop and 1, 2, 5, 10 years postop)
  • Patient-reported outcome: Forgotten Joint Score(1, 2, 5, 10 years postop)
  • Radiographic performance of the implants looking for radiolucencies, migration, loosening, subsidence(Immediately postop + 1, 2, 5, 10 years postop)
  • Intraoperative and postoperative Adverse events(Intraop + Immediately postop + 1, 2, 5, 10 years postop)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (5)

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