Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06502873

Setting up a Cohort of Patients With Inflammatory Bowel Disease and a Cohort of Patients Without Chronic Inflammatory Bowel Disease

Led by Artialis · Updated on 2026-01-28

120

Participants Needed

1

Research Sites

130 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Setting up a Cohort of Patients With Inflammatory Bowel Disease and a Cohort of Patients Without Chronic Inflammatory Bowel Disease

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female 18 years or older
  • Able to follow study instructions
  • Signed informed consent
  • Confirmed diagnosis of IBD for Crohn cohort
  • Rectal, colonic, or ileocolic involvement for Crohn cohort
  • Crohn patients with inflammatory flare and disease extent in colon or ileocolic region meeting clinical activity criteria
  • Endoscopic activity meeting SES-CD or CDEIS scores for Crohn cohort
  • Ulcerative colitis patients with inflammatory flare meeting clinical activity and endoscopic criteria
  • Control patients with no visible colonic lesions during endoscopy
Not Eligible

You will not qualify if you...

  • Use of commercial pharmaceutical probiotics within the last month
  • Antibiotic treatment within the past 3 months
  • Non-remission cancer or remission less than 6 months
  • Contraindications to colonoscopy or biopsy
  • Under guardianship or judicial protection
  • Pregnant or breastfeeding women
  • Participation in clinical study with investigational medicine or supplement in last 3 months
  • Crohn disease localized only in ileum
  • Inflammatory colon pathologies other than Crohn's

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CHU de Liège

Liège, Belgium

Actively Recruiting

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Research Team

B

Bérénice Costes

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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