跳至主要内容
临床试验/NCT03698071
NCT03698071已完成不适用

Soluble CD95 Ligand Role in the Pathophysiology of ANCA Associated Vasculitis

University Hospital, Bordeaux1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2018年12月14日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
48
试验地点
1
主要终点
Change of quantitative levels of s-CD95-L in ANCA associated vasculitis between baseline and Month 12

研究概览

简要总结

The study aims at defining the role of soluble CD95 Ligand in the physiopathology of a rare group of inflammatory diseases: ANCA associated vasculitis. Soluble CD95 Ligand might have a prognostic and diagnostic interest as well as potential for the discovery of new therapeutic strategies.

详细描述

ANCA associated vasculitis are a rare group of diseases and potentially life-threatening inflammatory conditions. There is an urgent need to describe prognostic factors and to discover new therapeutic pathways. Soluble CD95-L is a cleaved part of CD95-L which binds the CD95 Death receptor. s-CD95-L has pro-inflammatory properties for Th17 lymphocytes and Neutrophils, two cells implicated in ANCA associated vasculitis. It also plays a role in systemic lupus erythematosus (which present with the same type of renal glomerulonephritis as ANCA-associated vasculitis). Finally, it has already be found elevated in this group of diseases. The investigators hypothesized that s-CD95-L levels might be a prognostic factor in ANCA associated vasculitis and the study of the molecular mechanisms involved could provide new therapeutic targets.

The study will recruit 50 patients with ANCA associated vasculitis followed in Bordeaux University Hospital. Among classical disease activity information, blood and urine samples will be collected at each visit to study s-CD95-L. Fundamental research will be realized on patients' sample to study molecular mechanisms involved.

Clinical and biological disease activity, treatment and outcomes will be studied in correlation with s-CD95-L to describe their potential prognostic role. Patients will be followed at regular intervals, as their usual follow-up would request. No extra visit will be needed and blood samples will be drawn at the same time as those drawn for clinical purposes.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

  • Diagnosis of ANCA associated vasculitis according to the Chapel-Hill Consensus Conference - 2012 modified version
  • Age ≥ 18 years
  • being affiliated to health insurance
  • willing to participate and to sign informed consent.

排除标准

  • Pregnant or breastfeeding women,
  • patient concerned by articles L 1121-5 to L 1121-8 (persons deprived of their liberty by a judicial or administrative decision, minors, persons of legal age who are the object of a legal protection measure or unable to express their consent)

研究组 & 干预措施

ANCA associated vasculitis

Experimental

干预措施: blood sample (Biological)

ANCA associated vasculitis

Experimental

干预措施: urine sample (Biological)

结局指标

主要结局

Change of quantitative levels of s-CD95-L in ANCA associated vasculitis between baseline and Month 12

时间窗: At baseline (Day 0) and 12 months from baseline

次要结局

  • Change of quantification of ANCA in the blood samples of ANCA associated vasculitis between baseline and Month 12(At baseline (Day 0) and 12 months from baseline)
  • Change of quantification of s-CD95-L in the blood and urine samples of ANCA associated vasculitis between baseline and Month 12(At baseline (Day 0) and 12 months from baseline)
  • Change of disease activity scores for ANCA associated vasculitis between baseline and Month 12(At baseline (Day 0) and 12 months from baseline)

研究者

发起方
University Hospital, Bordeaux
申办方类型
Other
责任方
Sponsor

研究点 (1)

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