跳至主要内容
临床试验/NCT02868645
NCT02868645已完成不适用

Interest of Serum Periostin Dosage in Patients With Bone Fibrous Dysplasia

Hospices Civils de Lyon1 个研究点 分布在 1 个国家目标入组 65 人开始时间: 2016年5月25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
入组人数
65
试验地点
1
主要终点
Periostin rate in serum

研究概览

简要总结

Fibrous dysplasia is a rare bone disease which can cause pain and fractures. It has been shown that periostin is over expressed in fibrous component in patients bones ; but periostin has never been measured out in serum of patients, although it is easy to assess. This study aims to show whether serum periostin is elevated in serum of patients with fibrous dysplasia, and if it is more elevated in patients with severe forms of the disease.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

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

入选标准

  • patients with fibrous dysplasia of the bone
  • access to social security
  • informed consent

排除标准

  • no informed consent
  • pregnancy
  • patients with a history of conditions known to increase periostin serum (stade IV cancer, severe asthma, pulmonary fibrosis…)

研究组 & 干预措施

Patients with bone fibrous dysplasia

Experimental

Patients with bone fibrous dysplasia will have a blood sampling to assess periostin rate in serum

干预措施: Blood sampling (Biological)

结局指标

主要结局

Periostin rate in serum

时间窗: At inclusion

次要结局

  • Periostin rate in serum in patients with Mac Cune Albright syndrome(At inclusion)
  • Periostin rate in serum according to the number of fibrotic bones(At inclusion)
  • Periostin rate in serum in patients with severe phenotype of the disease(At inclusion)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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