跳至主要内容
临床试验/NCT02065297
NCT02065297已完成不适用

Quantitative and Functional Study of TH17 Lymphocytes in Horton's Disease (HD)

Centre Hospitalier Universitaire Dijon3 个研究点 分布在 1 个国家目标入组 143 人开始时间: 2009年7月28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
143
试验地点
3
主要终点
Quantification of specific cytokines of the Th17 immune response (IL-17 A and IL-23) in the serum

研究概览

简要总结

The aim of this open, controlled, multicentre biomedical research study is to identify new markers specifically associated with Horton's disease. This would make it possible to improve the diagnosis and management of this disease.

Participation consists in taking one or several blood samples depending on the group patients/controls.

研究设计

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

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients who have provided written informed consent
  • Patients with national health insurance cover
  • Age: 50 to 90 years
  • Patients with Horton' s disease :
  • at the diagnosis, before any treatment
  • or in remission
  • or in relapse
  • Patients with an infectious disease :
  • Bacteriologically or radiologically confirmed
  • Presenting an inflammatory syndrome defined by :
  • CRP ≥ 10 mg / L
  • and Fibrinogen ≥ 4 g / L or ESR ≥ 30 mm at H1
  • Patients with neoplasia ( solid tumour or hemopathy ) :
  • At the diagnosis, before treatment by chemotherapy
  • Presenting an inflammatory syndrome defined by:
  • CRP ≥ 10 mg / L
  • and Fibrinogen ≥ 4 g / L or ESR ≥ 30 mm at H1
  • These are healthy volunteers recruited among blood donators at Dijon CHU, voluntary hospital personnel ( nurses, doctors and secretaries ), patients at the EPHAD ( Champmaillot centre for geriatric patients ) and patients without infectious, inflammatory, or auto-immune disease ( CRP < 5mg / L ) or cancer recruited from the investigating departments of Dijon CHU. They will be matched for age and sex.
  • Age: 18 - 90 years
  • Patients with national health insurance cover
  • who have provided written informed consent
  • Absence of an inflammatory syndrome ( CRP < 5 mg / L )
  • Exclusion Criteria :
  • Any patient who does not meet the inclusion criteria

排除标准

  • 未提供

结局指标

主要结局

Quantification of specific cytokines of the Th17 immune response (IL-17 A and IL-23) in the serum

时间窗: Up to 6 months

Measurement of the activation level of genes specifically involved in Th17 response using RT-PCR on frozen mRNA

时间窗: Up to 6 months

Quantification of LTh17 by flow cytometry

时间窗: Up to 6 months

Measure the ability of Treg to proliferate and to synthesize IL-17 in response to different antigenic stimulations

时间窗: Up to 6 months

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 (3)

Loading locations...

相似试验