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临床试验/NCT04267510
NCT04267510已完成不适用

Clinical and Molecular Aspects of Early Osteoarthritis

University Hospital, Montpellier1 个研究点 分布在 1 个国家目标入组 65 人开始时间: 2013年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
65
试验地点
1
主要终点
identification of genetic mutation

研究概览

简要总结

The etiology of osteoarthritis is varied, ranging from multifactorial, environmental to monogenic. In individuals in whom osteoarthritis appears earlier than in the general population, it is called early osteoarthritis. To our knowledge, there are no large-scale genetic studies on people with early osteoarthritis. The investigators therefore sought to study the causes of monogenic osteoarthritis in people suffering from early non-syndromic osteoarthritis.

Material and method From 2013 to 2019, experts in constitutional bone disease sent patients with non-syndromic early osteoarthritis for genetic analysis to our center of competence for constitutional bone diseases. The sequencing of a panel of genes was carried out by NGS.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Other

入排标准

年龄范围
7 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with early osteoarthritis who have undergone genetic sequencing

排除标准

  • Patients refusing to participate in research

结局指标

主要结局

identification of genetic mutation

时间窗: 1 day

sequencing out by NGS

number of genetic mutation

时间窗: 1 day

sequencing out by NGS

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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