NCT06972901Recruiting
Evaluation of Therapeutic Strategy to Prevent Crohn's Disease Endoscopic poSToperatIve recurreNce Based on earlY Dosage of Faecal Calprotectin
Source: ClinicalTrials.gov · Last updated 5 Jun 2026
Brief summary (registry, in English)
Crohn's disease (CD) (\> 200,000 patients in France) is a chronic inflammatory disease that can lead to progression of intestinal destruction and impaired quality of life. Despite the widespread use of biotherapies, intestinal resections remain frequent (50% of patients over time). Unfortunately, surgery is not curative since 75% of patients experienced post-endoscopic operative recurrence (POR) (i.e., recurrence of ulcerations) during the first year after surgery. Prevention of endoscopic POR (defined as a Rutgeerts index ≥ i2) is essential because endoscopic POR is highly predictive of clinical POR (i.e., recurrence of CD-related symptoms): \> 40% and \> 80% within 5 years for a Rutgeerts index ≥ i2 or ≥ i3, respectively. The recommended management is to start treatment after surgery to avoid endoscopic POR, and to perform a colonoscopy at 6 months (M6) with therapeutic escalation if endoscopic POR. Despite anti-TNF or ustekinumab treatment, the endoscopic POR rate remains high (30-40% at M6) leading to \> 40% clinical POR despite therapeutic escalation (90 mg/4 weeks with ustekinumab) potentially due to late therapeutic escalation. Innovative strategies are therefore needed to prevent endoscopic POR, such as the use of fecal calprotectin, a non-invasive biomarker associated with endoscopic CD activity. We have previously demonstrated that its variation between surgery and M3 allows for a value at M3 predictive of endoscopic POR at M6. In this study, we hypothesize, for the first time, that a strategy integrating fecal calprotectin measurement at M3 with earlier therapeutic escalation (M3 vs M6) in case of abnormal value or kinetics could decrease the rate of endoscopic POR at M6.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 42 (estimated)
- First submitted
- 7 May 2025
- Start date
- Oct 2025
- Primary completion date
- Mar 2027
- Lead sponsor
- University Hospital, Clermont-Ferrand
- Diseases
- Crohn's disease
- NCT number
- NCT06972901
What you commit to
- Study type: Interventional
- Planned participants: 42
- From Oct 2025 to the primary completion date, Mar 2027
- 8 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Age
- Pregnant or breastfeeding women: a pregnancy test will be performed for women of childbearing age
Other
- Permanent stoma
- Total colectomy
- Uncontrolled postoperative infectious complication
- Refusal to participate in the study
- Persons deprived of their liberty by judicial or administrative decision
- Minors
- Vulnerable protected adults (under guardianship, curatorship, or legal protection)
Who the study is looking for
- Patients with an established diagnosis of CD according to ECCO guidelines
- Adult Crohn's disease (age ≥ 18 years)
- Having undergone ileal, colonic, or ileocolonic resection without residual macroscopic lesions
- With an anastomosis that can be reached by ileocolonoscopy
- With at least one of the following risk factors for endoscopic POR: active smoking, previous intestinal resection (before the current resection), length of resected small bowel \> 30 cm, fistulizing phenotype (B3 according to the Montreal classification), exposure to at least two biotherapies before surgery
- No contraindication to ustekinumab treatment
- Patient capable of giving consent
- Patient covered by the French healthcare system
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (8)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU D'amiens Coordinator of this site? Confirm its status | Amiens | France | Not yet recruiting |
| CHU de Clermont-Ferrand Coordinator of this site? Confirm its status | Clermont-Ferrand | France | Recruiting |
| CHU de Lille Coordinator of this site? Confirm its status | Lille | France | Not yet recruiting |
| HCL Coordinator of this site? Confirm its status | Lyon | France | Not yet recruiting |
| AP-HM Coordinator of this site? Confirm its status | Marseille | France | Not yet recruiting |
| CHU de Montpellier Coordinator of this site? Confirm its status | Montpellier | France | Not yet recruiting |
| CHU de Nice Coordinator of this site? Confirm its status | Nice | France | Not yet recruiting |
| CHU de Toulouse Coordinator of this site? Confirm its status | Toulouse | France | Not yet recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.