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临床试验/NCT03277989
NCT03277989终止不适用

INFINITY™Total Ankle Replacement Follow-up

Stryker Trauma and Extremities9 个研究点 分布在 1 个国家目标入组 155 人开始时间: 2017年10月9日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
155
试验地点
9
主要终点
Survivorship at 10 Years

研究概览

简要总结

Study Title INFINITY™Total Ankle Replacement Follow-up (ITAR) Study Design Prospective, multi-site, multi-year post-market clinical follow-up study Study Group Primary/Unilateral and/or bilateral Total Ankle Arthroplasty subjects implanted with INFINITY™ Total Ankle System Number of Subjects 150 with 9 sites

详细描述

The primary outcome measure of this post-market clinical observational study is to collect data relating to the INFINITY™ Total Ankle System survivorship at 10 years. The secondary outcome measures are to characterize the improvements after implantation over a 10 year period using patient reported outcome measures related to quality of life, pain and functional improvements, safety of the implants, as well as radiographic assessments (X-Rays)

The outcome measures collected in this study will be analyzed and reported as required for local, regional, and country requirements (i.e., regulatory authorities and notified bodies).

研究设计

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

入排标准

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

入选标准

  • Be 21 years of age or older at the time of surgery;
  • Diagnosed with unilateral and/or bilateral ankle joint disease;
  • Diagnosed with ankle joint damage from rheumatoid arthritis, post-traumatic, or degenerative arthritis;
  • Willing and able to consent to participate (written, informed consent;
  • Willing and able to attend the requested follow-up visits;
  • A clinical decision has been made to use INFINITY™ Total Ankle System replacement prior to enrollment in the research.

排除标准

  • Subjects with an ankle condition, as determined by the investigator, to be an inappropriate candidate for a total ankle replacement;
  • Subjects requiring revision total ankle replacement of the ankle being considered for study.

结局指标

主要结局

Survivorship at 10 Years

时间窗: 10 years

The primary endpoint is a survivorship rate at 10 years as defined with a Kaplan Meier survivorship analysis.

次要结局

  • Radiographic Evaluation-physician Reported Questionnaire(Pre-op through 2 years)
  • Ankle Osteoarthritis Score (AOS)(Pre-op though 2 years)
  • PROMIS Scale v1.2- Global Health(2 years)
  • FAOS Questionnaire(2 years)
  • TAR Satisfaction Questionnaire(Pre-op through 2 years)

研究者

发起方
Stryker Trauma and Extremities
申办方类型
Industry
责任方
Sponsor

研究点 (9)

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