NCT03107390
Terminated
Not Applicable
Evaluation of NT-proBNP in Chronic Inflammatory Bowel Disease
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Inflammatory Bowel Diseases
- Sponsor
- Centre Hospitalier Universitaire, Amiens
- Enrollment
- 159
- Locations
- 1
- Primary Endpoint
- Blood level of NTproBNP.
- Status
- Terminated
- Last Updated
- 5 years ago
Overview
Brief Summary
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.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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
Exclusion Criteria
- •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)
Outcomes
Primary Outcomes
Blood level of NTproBNP.
Time Frame: 1 month
Study Sites (1)
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