Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06690632

WAter Preparation in Crohn's Disease's Imagery

Led by University Hospital, Toulouse · Updated on 2026-05-08

194

Participants Needed

1

Research Sites

200 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to compare distension quality and patient experience of water and polyethylene glycol preparation as oral contrast media in Magnetic Resonance Enterography (MRE) in patients with Crohn's disease. Thus, the main question it aims to answer is: Is water sufficient to interpret MRE from patients with Crohn's disease? Researchers will compare the standard protocol (polyethylene glycol) with water as bowel distension agent to see if it is possible to obtain a satisfying global distension of small bowel. Participants will undergo the same procedures as standard care adding questionnaires and replacing water as the bowel distension agent for the MRE for patient randomized into the experimental group.

CONDITIONS

Official Title

WAter Preparation in Crohn's Disease's Imagery

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of Crohn's Disease
  • Need for Magnetic Resonance Enterography (MRE) as determined by patient's gastroenterologist
Not Eligible

You will not qualify if you...

  • Younger than 18 years old
  • Unable to provide informed consent
  • Under guardianship or curatorship
  • Allergy to polyethylene glycol (PEG)
  • Contraindications to MRE such as pregnancy, pacemaker, or claustrophobia
  • Contraindication to phloroglucinol administration (phenylcetonuria)
  • Contraindication to gadolinium administration including kidney failure with glomerular filtration rate below 30/mL/1.73m², pregnancy, or allergy

AI-Screening

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Trial Site Locations

Total: 1 location

1

CHU Toulouse

Toulouse, France

Actively Recruiting

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Research Team

G

Guillaume Dr LE COSQUER, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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