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The objective of this study is to constitute cohorts of IBD versus non-IBD patients to identify (a) new biomarker(s) of intestinal dysbiosis associated with inflammatory bowel disease, and develop a prototype for assaying such marker(s) in blood.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Inflammatory bowel disease cohort | Other | 60 patients diagnosed with colonic inflammatory bowel disease |
|
| Control cohort | Other | 60 control patients without inflammatory bowel diseases |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| biological samples collection | Procedure | Collection of biological samples from the same cohorts: faeces, serum, intestinal biopsies |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of patients recruited in each cohort | 60 patients in IBD cohort and 60 patients in control cohort | 27 months |
| number of faeces samples collected in each cohort | 60 patients in IBD cohort and 60 patients in control cohort | 27 months |
| Number of plasma samples collected in each cohort | 60 patients in IBD cohort and 60 patients in control cohort | 27 months |
| Number of biopsy samples collected in each cohort | 60 patients in IBD cohort and 60 patients in control cohort with 4 colonic biopsies/ patient | 27 months |
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Inclusion Criteria:
General criteria:
Specific for Crohn cohort:
A clinical activity defined by a modified Mayo score ≥ 3 OR a Simple Clinical Colitis Activity Index ≥5 OR Patient Reported Outcome (PRO2) ≥ 4 with a subscore of rectal bleeding ≥1 OR a faecal calprotectin ≥ 250 µg/g AND An endoscopic activity defined by a Mayo endoscopic sub-score ≥ 2
Specific for Control cohort:
Patient with no colonic lesion(s) visible during the endoscopical examination (neither Crohn's nor other colitis nor cancer)
Exclusion Criteria:
General criteria:
Specific for Crohn cohort:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Bérénice Costes | Contact | 042670888 | berenice.costes@artialis.com |
| Name | Affiliation | Role |
|---|---|---|
| Catherine Van Kemseke, MD | Centre Hospitalier Universitaire de Liege | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU de Liège | Recruiting | Liège | Belgium |
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| ID | Term |
|---|---|
| D015212 | Inflammatory Bowel Diseases |
| ID | Term |
|---|---|
| D005759 | Gastroenteritis |
| D005767 | Gastrointestinal Diseases |
| D004066 | Digestive System Diseases |
| D007410 | Intestinal Diseases |
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Prospective, monocentric, study aiming to recruit 2 types of patients (60 inflammatory bowel disease (IBD) suffering patients versus 60 control patients without IBD nor any other known intestinal pathology).
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