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临床试验/NCT03129230
NCT03129230已完成不适用

Yulin Orthopedics Hospital of Chinese and Western Medicine

Yulin Orthopedics Hospital of Chinese and Western Medicine2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2012年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
16
试验地点
2
主要终点
change of peri-implant bone level from baseline at 7 and 54 months

研究概览

简要总结

This study was to evaluate the safety and efficacy of free nonvascularized fibula autograft in the treatment of the femoral neck tumor-like lesions before epiphyseal closure in pediatric patients, by presenting the clinic-radiological outcome and complications.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
7 Years 至 13 Years(Child)
性别
All
接受健康志愿者

入选标准

  • This retrospective study included pediatric patients before epiphyseal closure with tumor-like lesions in femoral neck.

排除标准

  • pediatric patients with tumor-like lesions in femoral neck after epiphyseal closure;
  • pediatric patients with benign bone tumors and malignant bone tumors in the femoral neck after epiphyseal closure;
  • adult patients with benign or malignant bone tumors and tumor-like lesions in femoral neck.

研究组 & 干预措施

Free nonvascularized fibula autograft

Experimental

Sixteen pediatric patients before epiphyseal closure were treated with free nonvascularized fibula autograft after resections of tumor-like lesions in the femoral neck.

干预措施: free nonvascularized fibula autograft (Procedure)

结局指标

主要结局

change of peri-implant bone level from baseline at 7 and 54 months

时间窗: 7 months to 54 months

Mean follow-up of all the patients after primary surgery was 24 months, ranged 7 months to 54 months.

次要结局

未报告次要终点

研究者

发起方
Yulin Orthopedics Hospital of Chinese and Western Medicine
申办方类型
Other
责任方
Principal Investigator
主要研究者

Shanchao Luo

Director

Yulin Orthopedics Hospital of Chinese and Western Medicine

研究点 (2)

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