MRE: Magnetic Resonance Enterography at year 1 (in some patients)
Study summary
The investigators propose to create a prospective Crohn Disease cohort, where patients receiving the most up-to-date therapies with a treat-to-target strategy, will be closely followed to characterize the progression of Crohn Disease by measuring the Lémann Index over time. The goal of the CROCO Study - "Crohn's Disease Cohort Study" is to promote a greater understanding of the long-term evolution of Crohn Disease , to describe prospectively the impact of different therapeutic strategies and develop accurate predictors of bowel disease damage and disability.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
INCLUSION CRITERIA
To be eligible all of the following criteria must be met:
* Diagnosis of CD (according to ECCO guidelines) established within the past 12 months;
* Patients able to understand the information provided to them and to give written informed consent for the study;
* Male or female, age \> 18 years.
EXCLUSION CRITERIA:
* Patients unwilling or unable to provide informed, written consent;
* Severe underlying medical disorder with an anticipated life expectancy \< 2 years;
* Refusal or medical conditions (e.g. Glomerular filtration rate \< 30 mL/min) preventing cross-sectional imaging during follow-up;
* Uncertain CD diagnosis;
* Pregnancy (if it is impossible to implement the MRE at one year) or any other reason that makes resonance not feasible throughout the study (eg claustrophobia).
Primary outcome measure(s)
Lémann Index Y1 — 1 year after diagnosis The Lémann Index (LI) was developed to provide a tool to measure bowel damage in Crohn Disease (CD).
Descriptive statistics will present quantitative variables as mean and standard deviation or median and interquartile range (depending on their distribution) and qualitative variables as count and percentage.
Time to event endpoints (such as surgery and hospitalization) will be presented using cumulative incidence in a competing risk framework (with death without surgery as a competing event for time to surgery, for example). Cumulative incidence with its 95%CI will be estimated at meaningful timepoints and association between baseline predictors and time to event endpoint will be assessed using competing risks regression models. Correlation of LI and IBD-DI will be estimated, taking into account the repeated measurements.
Lémann Index is a continuous variable.
Lémann Index Y3 — 3 years after diagnosis The Lémann Index (LI) was developed to provide a tool to measure bowel damage in Crohn Disease (CD).
Descriptive statistics will present quantitative variables as mean and standard deviation or median and interquartile range (depending on their distribution) and qualitative variables as count and percentage.
Time to event endpoints (such as surgery and hospitalization) will be presented using cumulative incidence in a competing risk framework (with death without surgery as a competing event for time to surgery, for example). Cumulative incidence with its 95%CI will be estimated at meaningful timepoints and association between baseline predictors and time to event endpoint will be assessed using competing risks regression models. Correlation of LI and IBD-DI will be estimated, taking into account the repeated measurements.
Lémann Index is a continuous variable.
Lémann Index Y5 — 5 years after diagnosis The Lémann Index (LI) was developed to provide a tool to measure bowel damage in Crohn Disease (CD).
Descriptive statistics will present quantitative variables as mean and standard deviation or median and interquartile range (depending on their distribution) and qualitative variables as count and percentage.
Time to event endpoints (such as surgery and hospitalization) will be presented using cumulative incidence in a competing risk framework (with death without surgery as a competing event for time to surgery, for example). Cumulative incidence with its 95%CI will be estimated at meaningful timepoints and association between baseline predictors and time to event endpoint will be assessed using competing risks regression models. Correlation of LI and IBD-DI will be estimated, taking into account the repeated measurements.
Lémann Index is a continuous variable.
Trial sites (19)
Facility
City
Region
Status
University Hospital CHU of Liège
Liège
Liège
American Gastroenterology Center
Stróvolos
Cyprus
IBD Clinical and Research Clinic, ISCARE
Prague
Czechia
Hvidovre Hospital
Hvidovre
Denmark
Slagelse Hospital
Slagelse
Denmark
CHU Amiens-Picardie Hôpital Sud
Amiens
France
CHU Estaing Clermont - Ferrand
Clermont-Ferrand
France
Claude Huriez Hospital, Lille University
Lille
France
Azienda Ospedaliera di Padova
Padova
Italy
Mater dei hospital
Msida
Malta
Hospital Garcia da Orta
Almada
Almada
Instituto Portugues de Oncologia de Lisboa
Lisbon
Lisbon District
Hospital Beatriz Angelo
Loures
Loures
Algomed Policlinic
Timișoara
Romania
Hospital Clinic Barcelona
Barcelona
Spain
Hospital Galdakao-Usansolo
Galdakao
Spain
Hospital Alvaro Cunqueiro - Área Sanitária de Vigo
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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