Ileal Crohn's Disease and Post-operative Outcome: Prospective Cohort Study of the REMIND Group
Condition(s) studied
Investigational drug(s) / intervention(s)
bio-banking collection: blood samples, biopsies, and surgical specimen collected in addition to usual practice
Study summary
Crohn's disease (CD), a chronic inflammatory process in intestinal segments leads to tissue damage. More than two thirds of CD patients need intestinal resection. Symptomatic clinical recurrence occurs in 60% by 10 years. The principal factors affecting postoperative recurrence are active smoking, penetrating disease, perianal lesions history, prior intestinal resection, small bowel resection extent, and prophylaxis treatment absence.
Ileocolonoscopy within one year of surgery can predict clinical recurrence risk.
Different therapies are proposed after surgery, to prevent post-operative recurrence : Thiopurines, 6-mercaptopurine (positive for clinical and endoscopic postoperative recurrence prevention), Anti-tumour necrosis factor therapy (anti-TNF), the most effective therapy.
Intestinal microbiota acts as a central factor in the CD pathogenesis, and fecal stream role is clearly shown. Various changes in luminal flora with a possible link to local inflammation was also demonstrated. Bacteria associated with postoperative recurrence could be more pathogenic as adherent invasive E coli (AIEC), which could be a pathogen in CD through several mechanisms including increased mucosal colonization, adherence, replication and induction of TNF secretion. Alternatively, postoperative CD recurrence could be linked to a protective commensal species lack, such as Faecalibacterium prausnitzii.
Microscopic inflammation occurs as early as 8 days after anastomosis in the neoterminal ileum mucosa. IL6, IL10 and TGFb levels, measured in neoterminal ileum early after surgery are associated with different rates of postoperative recurrence. It suggests cytokines implication in postoperative recurrence. T cells are major players in the intestinal immune response. The presence at time of surgery and persistence of disease inducing T cell clonal expansions could play an important role in post-operative recurrence.
The main objective is to define a classification of ileal Crohn's Disease based on data integration on a large cohort of patients.
Eligibility
Primary outcome measure(s)
- Ileal Crohn's disease classification — surgery time, Time 0
Ileal Crohn's disease classification will be performed using data integration (taking into account clinical data, immunological, genetic, microbiota, transcriptome data). A molecular classification will be possible due to this data integration analysis - Postoperative recurrence study — 6 months after surgery
Rates of endoscopic recurrence as defined by a Rutgeerts score ≥ 1 in patients will be evaluated at the endoscopic exam - Study of Treatments efficacy to prevent recurrence — 6 months after surgery time
During a clinical visit, scheduled as usual practice 6 months after surgery, clinical data will be collected : treatment modification or optimization, recurrence occurrence. If treament modification or optimization is needed (clinical symptoms or endoscopic recurrence), or complication occurs (abcess, occlusive syndrom, new surgery), patient will be considered as suffering a long-term relapse - Identification of biomarkers which could predict postoperative recurrence and response to treatments — surgery time, Time 0
Identification of biomarkers taking into account clinical data, immunological, genetic, microbiota, transcriptome data
Trial sites (17)
| Facility | City | Region | Status |
|---|---|---|---|
| SART Tilman Hospital | Liège | Belgium | Recruiting |
| Amiens Hospital | Amiens | France | Recruiting |
| Haut-levêque Hospital | Bordeaux | France | Active Not Recruiting |
| Clermont-Ferrand Hospital | Clermont-Ferrand | France | Recruiting |
| Beaujon Hospital | Clichy | France | Recruiting |
| Henri Mondor Hospital | Créteil | France | Recruiting |
| Kremlin-Bicêtre Hospital | Le Kremlin-Bicêtre | France | Recruiting |
| Lille Hospital | Lille | France | Recruiting |
| Hôpital Nord, CHU Marseille | Marseille | France | Recruiting |
| Montpellier Hospital | Montpellier | France | Recruiting |
| Brabois Hospital | Nancy | France | Recruiting |
| Nantes Hospital | Nantes | France | Recruiting |
| Archet 2 Hospital | Nice | France | Recruiting |
| Saint Louis Hospital | Paris | France | Recruiting |
| Saint Antoine Hospital | Paris | France | Recruiting |
| South Lyon Hospital | Pierre-Bénite | France | Recruiting |
| Strasbourg Hospital | Strasbourg | France | Active Not Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT03458195 on ClinicalTrials.gov ↗ ← All trials in Belgium