Clinical Trials Directory

Trials / Completed

CompletedNCT06526234

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

Status
Completed
Phase
Study type
Observational
Enrollment
250 (actual)
Sponsor
Central Hospital, Nancy, France · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DEVICEMRIMR enterography

Timeline

Start date
2023-01-01
Primary completion
2023-05-31
Completion
2025-11-30
First posted
2024-07-29
Last updated
2026-01-28

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT06526234. Inclusion in this directory is not an endorsement.