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临床试验/NCT04209374
NCT04209374已完成不适用

Etude de Cohorte Observationnelle Rétrospective SYMBOL CUP 1

Dedienne Sante S.A.S.1 个研究点 分布在 1 个国家目标入组 59 人开始时间: 2014年7月3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
59
试验地点
1
主要终点
Implant survival: Ratio of the number of participants alive with the complete index hip prosthesis in position at 2-year follow-up, over their initial numberprosthesis in position at 2-year follow-up, over their initial number.

研究概览

简要总结

This is a single-center retrospective observational cohort study of consecutively operated patients who underwent primary total hip arthroplasty with a SYMBOL CUP DM HA hemispherical dual mobility acetabular implant. The purpose of this study is to estimate the safety and efficacy of that implant at two-year follow-up.

详细描述

Description according to PICOS framework:

Patients:

  • Adult men and women requiring a primary total hip arthroplasty

Intervention:

  • Primary THA with SYMBOL CUP DM HA hemispherical dual mobility acetabular implant.

研究设计

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

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

  • All patients with total hip implant using hemispheric dual-mobility SYMBOL CUP DM HA
  • Operation performed by the primary investigator
  • Delay between index operation and March 1 2018 has reached 2 years

排除标准

  • patient refusal to participate in the study
  • minors (age < 18 years)
  • patients under guardianship

结局指标

主要结局

Implant survival: Ratio of the number of participants alive with the complete index hip prosthesis in position at 2-year follow-up, over their initial numberprosthesis in position at 2-year follow-up, over their initial number.

时间窗: 2 years as of index operation

This is the ratio of the number of participants who are alive with the complete index hip prosthesis in position at a given follow-up time (numerator) over the initial number of those participants from the date they received the index hip prosthesis (denominator). The cumulative ratio is recalculated at each event using the Kaplan-Meier method from the date of each participant index operation through the date of each participant's death or prosthetic removal surgery or loss-to-follow-up or last assessment alive with the hip prosthesis in place. The longest duration between the index operation and the final assessment is 2 years.

次要结局

  • Number of patients with one or several post-operative adverse events and count of each Serious adverse event and aggregate count of adverse events(2 years as of index operation)
  • Harris Hip Score (HHS) at baseline and 1-year follow-up(1 year as of index operation)
  • The modified Harris Hip Score (modified HHS) at baseline, 1-year and 2-year follow-up(2 years as of index operation)
  • Devane classification at baseline, 1-year and 2-year follow-up.(2 years as of index operation)
  • Charnley classification at baseline, 1-year and 2-year follow-up.(2 years as of index operation)

研究者

发起方
Dedienne Sante S.A.S.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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