NCT03510065已完成不适用
Post Market Clinical Follow-Up Study Prevision®
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Aesculap AG
- 入组人数
- 150
- 试验地点
- 1
- 主要终点
- Prevision® survival
研究概览
简要总结
Monocentric, non-interventional Post-Market Clinical Follow-Up (PMCF) Study on past implantations of the Prevision® prosthesis; the survival rate of the Prevision® prosthesis shall be evaluated and compared to literature results on comparable Revision stems.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
结局指标
主要结局
Prevision® survival
时间窗: 4-14 years after implantation
Kaplan Meier Survival Rate, retrospective Analysis of Patients operated between 2002 and 2012
次要结局
- Sinking / Migration of the Stem(4-14 years after implantation)
- Adverse Events(4-14 years after implantation)
- Serious Adverse Events(4-14 years after implantation)
- Clinical Results(4-14 years after implantation)
- Radiological Evaluation of the Stem(4-14 years after implantation)
- Pain(4-14 years after implantation)
- Ectopic Ossification(4-14 years after implantation)
- Quality of Life(4-14 years after implantation)
研究者
研究点 (1)
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