NCT01833962Unknown不适用
A Retrospective Study of Actifuse Synthetic Bone Graft Versus Other Bone Graft Substitutes in Patients Requiring Lumbar Fusion
OrthoGeorgia1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2013年1月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Achievement of fusion prior to or at 12 months postoperatively
研究概览
简要总结
The purpose of this study is to assess fusion status in patients who underwent spinal fusion with Actifuse synthetic bone graft versus other bone graft material (including autograft) in achieving lumbar spinal fusion.
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
- 是
入选标准
- •Any patient 18 years of age or older
- •Patients with a minimum follow up of 1 year
- •Patients who have previously undergone TLIF, PLIF,PLF, XLIF procedures
排除标准
- •Patients under the age of 18
- •Any patient with less than 1 year of follow up history at the time of first data analysis
- •Any patient that the primary investigator deems as an unfit candidate
结局指标
主要结局
Achievement of fusion prior to or at 12 months postoperatively
时间窗: 6 - 12 months year
次要结局
未报告次要终点
研究者
研究点 (1)
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