NCT00588887终止不适用
Total Knee Replacement With Duracon® and Vanguard™ Prostheses
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 150
- 试验地点
- 1
- 主要终点
- Range of motion, Knee Society Score, Duration of surgery
研究概览
简要总结
The purpose of this study is to compare range of motion, Knee Society Scores, and duration of surgery for different total knee prostheses.
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 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved.
- •Patients requiring correction of varus, valgus, or posttraumatic deformity.
- •Patients requiring correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure.
排除标准
- •Patients with infection, sepsis, or osteomyelitis.
结局指标
主要结局
Range of motion, Knee Society Score, Duration of surgery
时间窗: 1 year
次要结局
未报告次要终点
研究者
研究点 (1)
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