The Crohn's Disease Endoscopic Index of Severity is a validated index to assess the severity of ileocolonic lesions. Depth of ulcerations are evaluated in each segment of ileocolon and the surface of lesions and ulcerations are reported on a 10-cm analogic scale. The Crohn's Disease Endoscopic Index of Severity is the main score used in controlled trials to assess the endoscopic severity of lesions in Crohn's Disease. The investigators aim to conduct a prospective pilot study primarily to evaluate the applicability of the Crohn's Disease Endoscopic Index of Severity to data obtained by the colonic capsule endoscopy procedure, provided that conventional ileo-colonoscopy and capsule endoscopy lead to comparable overall severity evaluations. Secondary objectives are to assess reproducibility of the reading of data obtained by CCE and to compare these data with those obtained by conventional ileocolonoscopy. If overall severity evaluations derived from the two examinations are not comparable, the secondary objectives will be used in an attempt to understand the reasons of this discrepancy.
Twenty-four patients with CD will be included in the study on the basis of the need for an ileo-colonoscopy whatever the indication. * Males and females patients more than 18-years-old * Known colonic CD patients with a diagnosis based on established clinical, endoscopic, ra-diologic, and histologic criteria * Ileocolonoscopy scheduled * Patients' agreement for the CCE procedure to be performed within the week following the ileocolonoscopy. * Previous imaging of small bowel (one or more) by Small Bowel Follow Through (SBFT), Magnetic Resonance Enteroclysis (MRE) or Computed Tomography Enterography (CTE) performed in the last 12 months
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
24
Ileocolonic endoscopy scheduled; then colon capsule endoscopy performed.
Hopital Beaujon
Clichy, France
Chru Lille
Lille, France
Chu Nantes
Nantes, France
Data obtained by the colon capsule endoscopy as a Measure of safety
Time frame: 1 month
Reproducibility of the identification of the different anatomic segments on the CCE recordings
Time frame: 1 month
Reproducibility of the detection of each lesion
Time frame: At inclusion
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