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Performance of Non-injected MR Enterography Compared to a Conventional MR Enterography Protocol With Contrast Agent Injection (Fast-MR)

C

Central Hospital, Nancy, France

Status

Completed

Conditions

Crohn Disease

Treatments

Device: MRI

Study type

Observational

Funder types

Other

Identifiers

NCT06526234
2024PI153

Details and patient eligibility

About

Entero-MRI is indicated in Crohn's disease as part of the initial work-up or follow-up (to assess response to treatment, complications). The protocol for carrying out the examination complies with precise specifications set out in international recommendations. To perform the test, the small intestine must be distended with a hyperosmolar product. This protocol is applied to all patients, with no distinction or adaptation.

The total duration of the examination is sometimes difficult for patients to bear. Ingestion of the product to obtain distension of the small intestine is often poorly tolerated by patients.

In a number of cases, the entero-MRI may have been normal due to symptomatology regression or other diagnosis. The patient therefore underwent a complete examination similar to that of a patient with a pathology requiring characterization.

In this context, the investigators hypothesize that fast MR sequences are sufficient to discriminate between normal and abnormal examinations.

Enrollment

250 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

Patient with MR enterography examination for follow-up or suspected Crohn's disease

No Exclusion Criteria.

Trial design

250 participants in 1 patient group

Patients with Crohn's disease or suspected Crohn's disease
Treatment:
Device: MRI

Trial contacts and locations

1

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Central trial contact

Valérie LAURENT, MD-PhD; DROUOT Guillaume, PhD

Data sourced from clinicaltrials.gov

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