MRI scans may help prevent intestinal damage in Crohn's disease
NCT ID NCT04973423
First seen Jul 30, 2026 · Last updated Jul 31, 2026 · Updated 1 time
Summary
This trial tests whether adding regular MRI scans to standard monitoring (stool tests and symptom checks) can improve outcomes for people with Crohn's disease who are starting biotherapy. Crohn's is a chronic inflammatory bowel disease that can damage the full thickness of the intestinal wall, often leading to surgery. The study compares two groups: one receiving standard tight control with stool tests, and another also getting two additional MRI scans. The goal is to see if the MRI group spends more time in symptom-free remission without steroids.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- MRI scans added to standard monitoring
- What this could lead to
- If successful, adding MRI scans to standard monitoring could help prevent intestinal damage and reduce the need for surgery in Crohn's disease.
- What could go wrong
- This is a relatively small, early-stage trial, and the added benefit of MRI over standard monitoring may be modest. MRI is also more costly and less accessible than stool tests.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 180 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2022
- Expected to finish
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Aug 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult Crohn's disease (age ≥ 18 years) * Symptomatic with Crohn's disease activity index (CDAI)\> 150 * Presence of objective signs of inflammatory activity (fecal calprotectin\> 250 AND sign of MRI activity) * Requiring treatment with biotherapy according to the investigator * Able to give informed consent to participate in research * Affiliation to a Social Security scheme. Exclusion Criteria: * Severe obstructive symptoms * Uncontrolled intra-abdominal abscess * Isolated anoperineal lesions * Prevention of postoperative endoscopic recurrence * Temporary or definitive ostomy * Total colectomy * Contraindication to MRI * Pregnant or breastfeeding women * Protected adults (curatorship, guardianship, saving justice) * Refusal of participation
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
17 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Amiens university hospital
NOT_YET_RECRUITINGAmiens, France
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Aurillac Hospital
NOT_YET_RECRUITINGAurillac, France
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Bayonne hospital
NOT_YET_RECRUITINGBayonne, France
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Bordeaux university hospital
NOT_YET_RECRUITINGBordeaux, France
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Chambery Hospital
NOT_YET_RECRUITINGChambéry, France
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Clermont-Ferrand University hospital
RECRUITINGClermont-Ferrand, France
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Grenoble University Hospital
NOT_YET_RECRUITINGGrenoble, France
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Issoire Hospital
NOT_YET_RECRUITINGIssoire, France
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LILLE university hospital
NOT_YET_RECRUITINGLille, France
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Lyon Hospital, Hospices civils de Lyon
NOT_YET_RECRUITINGLyon, France
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Montluçon Hospital
NOT_YET_RECRUITINGMontluçon, France
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Montpellier University hospital
NOT_YET_RECRUITINGMontpellier, France
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Nancy University hospital
NOT_YET_RECRUITINGNancy, France
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Nice University hospital
NOT_YET_RECRUITINGNice, France
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Rennes University Hospital
NOT_YET_RECRUITINGRennes, France
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Saint Etienne University Hospital
NOT_YET_RECRUITINGSaint-Etienne, France
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Thiers Hospital
NOT_YET_RECRUITINGThiers, France
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Other studies related to the condition(s) this trial covers.
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