跳至主要内容
临床试验/NCT03107390
NCT03107390终止不适用

Evaluation of NT-proBNP in Chronic Inflammatory Bowel Disease

Centre Hospitalier Universitaire, Amiens2 个研究点 分布在 1 个国家目标入组 159 人开始时间: 2013年10月28日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
159
试验地点
2
主要终点
Blood level of NTproBNP.

研究概览

简要总结

NT-proBNP is a major diagnostic and prognostic marker in cardiology, but it is also a new marker for biological inflammation, especially in rheumatology.

Its evaluation in chronic inflammatory bowel disease was carried out in a preliminary study, the OPERA study where in a population of 12 patients showed an increase in NT-proBNP correlated with the biological and endoscopic activity of the disease. This larger study is therefore a pilot study that could see NTproBNP as a new biomarker of inflammation in MICI.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Prevention
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

  • Adult subjects (age 18 years)
  • MICI Group: Patients monitored for probable HC or MC
  • Control group: Patients referred for consultation in gastroenterology with a clinical and endoscopic picture eading to the diagnosis of TF I
  • Person who agreed to participate in the study
  • Patient covered by social insurance

排除标准

  • Causes of increased concentrations of natriuretic peptides: acute heart failure, acute or chronic pulmonary disease with right ventricular repercussion, valvulopathies, primary or secondary HVG, atrial fibrillation cardiac arrhythmia, chronic systolic dysfunction, hyperthyroidism, Addison's disease, hyperaldosteronism Primary, diabetes, cirrhosis with ascites, cancers, chronic renal insufficiency.
  • Inflammatory and autoimmune diseases (excluding MC and RCH), chronic inflammatory syndrome
  • Ongoing treatment that may affect the concentration of natriuretic peptides: ACE inhibitor, angiotensin II receptor antagonists, diuretics
  • Patient deprived of liberty or protected major (under guardianship or curatorship)

结局指标

主要结局

Blood level of NTproBNP.

时间窗: 1 month

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 (2)

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