NCT00935870已完成不适用
Bioactive Glass (S53P4) as Bone Graft Substitute in Operative Treatment of Depressed Lateral Condyle Fractures, Benign Bone Tumour Cavities and in Spinal Fusion - a 10 Years Follow-up and Bone Density Study.
Vivoxid Ltd1 个研究点 分布在 1 个国家目标入组 63 人开始时间: 2008年1月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 63
- 试验地点
- 1
研究概览
简要总结
The main aim is to evaluate the long-term safety and bone healing in the operated area and to compare bioactive glass granules with autogenous bone as a filler material.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Cross Sectional
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Written informed consent obtained; Participation of previous clinical investigation with bioactive glass
排除标准
- •The subject is unlikely to adhere to study procedures
- •Concurrent disease or condition that in the opinion of the investigator is contraindicating participation
- •Simultaneous participation in another medical device or investigational drug trial
研究者
研究点 (1)
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