NCT00764959终止不适用
Post-Market Study of the Linear™ Hip System
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 200
- 试验地点
- 1
- 主要终点
- The use and efficacy of the Encore Linear™ Hip System
研究概览
简要总结
The purpose of this study is to evaluate the use and efficacy of the Encore Linear™ Hip System in a group of 200 patients for whom data has already been collected.
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
- 否
入选标准
- •Have hip joint disease related to one or more of the following
- •osteoarthritis
- •rheumatoid arthritis
- •femoral fracture
- •correction of a functional deformity
- •avascular necrosis of the natural femoral head
- •Skeletal maturity
- •Patient is likely to be available for evaluation for the duration of the study
- •Able and willing to sign the informed consent and follow study procedures
- •Patient is not pregnant
- •No infection present
- •No known materials sensitivity
- •Patient is over 18 years of age
排除标准
- •Skeletal immaturity
- •Infection or sepsis
- •Insufficient bone quality that may affect the stability of the implant
- •Muscular, neurologic or vascular deficiencies which compromise the affected extremity
- •Alcoholism or other addictions
- •Prisoners
- •High levels of physical activity
- •Patient is pregnant
- •Loss of ligamentous structures
- •Materials sensitivity
- •Patient is under 18 years of age
结局指标
主要结局
The use and efficacy of the Encore Linear™ Hip System
时间窗: 2 year
次要结局
未报告次要终点
研究者
研究点 (1)
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