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临床试验/NCT02211794
NCT02211794进行中(未招募)不适用

A Prospective, Non-randomized, Consecutive Series, Multicenter, Observational Trial to Evaluate the Clinical Outcome of Total Knee Arthroplasty Using Journey II BCS Total Knee System

Smith & Nephew Orthopaedics AG5 个研究点 分布在 5 个国家目标入组 175 人开始时间: 2014年1月最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
175
试验地点
5
主要终点
Revision for any reason

研究概览

简要总结

Post-market study to confirm the safety and efficacy of the Journey II BCS knee prosthesis.

详细描述

Multicenter, prospective, observational study to collect relevant clinical data from 167 subjects implanted with the Journey II BCS Knee System. Data from eligible subjects, who have provided written informed consent for the collection of their coded data will be recorded from the patient's medical file on specially designed case report forms (CRF's).

Total study duration for participants will be 10 years with follow-up visits planned at 3 months, 1 year, 2 years, 5 years and 10 years post-surgery. An interim analysis describing the clinical outcome is planned after 5 years.

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

入选标准

  • 未提供

排除标准

  • age > 75 years
  • conditions that may interfere with the TKA survival or outcome (i.e., Paget's or Charcot's disease, vascular insufficiency, muscular atrophy, uncontrolled diabetes, moderate to severe renal insufficiency or neuromuscular disease)
  • subject has inadequate bone stock to support the device

结局指标

主要结局

Revision for any reason

时间窗: 10Years

The goal of this study is to confirm the safety and efficacy of the Journey II BCS knee prosthesis by demonstrating non-inferiority of the cumulative percent success in subjects implanted with the JOURNEY II BCS Total Knee System compared to a literature reference rate of 94.3% (AOA annual report 201121) at 10 years. "Success" is defined as 10 year survival of the study device without revision for any reason.

次要结局

  • complication rate (adverse events and revisions)(discharge, 3month, 1yr, 2yr, 5yr, 10yr)
  • 2011 Knee Society Score(pre-op, 3month, 1yr, 2yr, 5yr, 10yr)
  • radiographic evaluation(pre-op, discharge, 3month, 1yr, 5yr, 10yr)
  • EQ-5D questionnaire(pre-op, 3month, 1yr, 2yr, 5yr, 10yr)
  • Knee Pain Evaluation Form questionnaire(3month, 1yr, 2yr)

研究者

发起方
Smith & Nephew Orthopaedics AG
申办方类型
Industry
责任方
Sponsor

研究点 (5)

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