跳至主要内容
临床试验/NCT00872573
NCT00872573终止4 期

Prospective, Uncontrolled, Two-centre, RSA, Post-market Surveillance Study to Evaluate the Stability of the C-Stem™ AMT Femoral Component in Primary Total Hip Arthroplasty.

DePuy International1 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2006年7月1日最近更新:
适应症

试验速览

阶段
4 期
状态
终止
发起方
入组人数
5
试验地点
1
主要终点
Distal migration of the femoral stem at the 5-year time point

研究概览

简要总结

The purpose of this study is to monitor the stability of the C-Stem™ AMT hip within the thigh bone when used in the treatment of patients with hip joint disease requiring a total hip replacement. Patients who enter the study will be evaluated at regular intervals following hip surgery using patient, clinical, standard x-ray assessments and special x-rays which allow the stability of the implant to be determined.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
60 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • i) Male or female subjects, aged between 60 and 80 years inclusive.
  • ii) Subjects who are able to give voluntary, written informed consent to participate in this investigation and from whom consent has been obtained.
  • iii) Subjects who, in the opinion of the Investigator, are able to understand this investigation, co-operate with the investigational procedures and are willing to return to the hospital for all the required post-operative follow-ups.
  • iv) Subjects undergoing primary total hip replacement that are considered suitable for a cemented femoral stem and metal femoral head and an all polyethylene acetabular cup.

排除标准

  • i) Subjects who, in the opinion of the Investigator, have an existing condition that would compromise their participation and follow-up in this study.
  • ii) Subjects undergoing revision hip replacement
  • iii) Subjects undergoing simultaneous bilateral hip replacements.
  • iv) Subjects with a contralateral hip replacement, which was implanted less than six months previously or is not performing satisfactorily.
  • v) Women who are pregnant.
  • vi) Subjects who are known drug or alcohol abusers or with psychological disorders that could affect follow-up care or treatment outcomes.
  • vii) Subjects who have participated in a clinical study with an investigational product in the last 12 months.
  • viii) Subjects who are currently involved in any injury litigation claims.

结局指标

主要结局

Distal migration of the femoral stem at the 5-year time point

时间窗: 5 years

次要结局

  • Harris Hip score(3mths, 1yr, 2yrs, 5yrs and 10yrs post-surgery)
  • Oxford Hip score(3mths, 1yr, 2yrs, 5yrs and 10yrs post-surgery)
  • Radiological analysis(3mths, 1yr, 2yrs, 5yrs and 10yrs post-surgery)
  • ML/AP translation and all rotations out to 5 years(pre-discharge, 3mths, 6mths, 1yr, 18mths, 2yrs, 3yrs and 5yrs post-surgery)

研究者

发起方
DePuy International
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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