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Clinical Trial Summary

The project will consist of a multicentre, prospective, observational study with a total duration of 24 months. Clinical, endoscopic and ultrasound data will be collected in a dedicated database (on IG-IBD Register), which will be used to identify potential clinical, endoscopic and ultrasound risk factors of re-operation. These data could be merged into a shared score, to stratify patients according to the risk of post-surgical re- operation and to define an optimal therapeutic management in the post- operative period. Approximately 220 adult patients, with a defined diagnosis of CD, who underwent a surgery for CD in the previous 6 months will be enrolled.


Clinical Trial Description

Patients will be consecutively enrolled in this prospective cross-sectional study, during the first 12 months, and then followed for 12 (minimum) up to 24(maximum) months, depending on date of patients' enrolment (total study length: 2 years). Patients will be stratified according to risk factors and type of treatment carried out in that year ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03150238
Study type Observational
Source Istituto Clinico Humanitas
Contact Federica Furfaro, MD, PhD
Phone +390282245555
Email federica.furfaro@humanitas.it
Status Recruiting
Phase N/A
Start date April 13, 2017
Completion date May 31, 2019

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