The purpose of this study is to evaluate Cortiment® with regard to its use by clinicians in routine clinical practice and its effectiveness and tolerability in a real-life setting.
Study Type
OBSERVATIONAL
Enrollment
378
Digestive Health Clinic (there may be other sites in this country)
Richmond Hill, Canada
Magen-Darm-Zentrum, Facharztzentrum Eppendorf (there may be other sites in this country)
Hamburg, Germany
St. Vincent's University Hospital (there may be other sites in this country)
Dublin, Ireland
Clinical benefit in routine practice, defined as % of patients with clinical improvement ≥ 3-point in Ulcerative Colitis Disease Activity Index (UCDAI) clinical sub-score
Time frame: From Day 1 to end of induction treatment (recommended duration up to 8 weeks)
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Investigational site (there may be other sites in this country)
Bologna, Italy
Investigational site (there may be other sites in this country)
Amsterdam, Netherlands
Investigational site (there may be other sites in this country)
Warsaw, Poland
Danderyds sjukhus (there may be other sites in this country)
Stockholm, Sweden
Kings College Hospital (there may be other sites in this country)
London, United Kingdom