The study prospectively compares two treatment algorithms for newly diagnosed Crohn's disease: one 'aggressive' treatment with early introduction of immunomodulators and biologicals and one 'standard treatment' with corticosteroids and only later introduction of immunosuppressives and biologicals if disease activity requires that.
This two year open-label randomized trial compares the early use of combined immunosuppression to conventional management in patients with active Crohn's disease who have not previously received glucocorticoids, antimetabolites, or infliximab. Patients assigned to combined immunosuppression receive azathioprine and 3 infusions of 5 milligrams per kilogram of body weight of infliximab at weeks 0, 2, and 6. Retreatment with infliximab and, if ultimately necessary, corticosteroids are used to control disease activity. Patients assigned to conventional management receive corticosteroids followed, in sequence, by azathioprine and infliximab. The primary outcome measure is remission without corticosteroids and without bowel resection at weeks 26 and 52.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
129
infliximab 5 mg/kg at week 0,2 and 6 + azathioprine 2-2.5 mg/kg
methylprednisolone 32 mg followed by taper or budesonide 9 mg/day followed by taper
Imelda GI Clinical Research Center
Bonheiden, Belgium
remission without corticosteroids and without surgical resection
Time frame: month 6 and 12 after inclusion
the time to relapse after successful induction therapy
Time frame: within 24 months
the proportion of patients receiving infliximab, methylprednisolone and antimetabolites
Time frame: within 24 months
the median serum C-reactive protein concentration
Time frame: 24 months
the proportion of patients experiencing adverse events
Time frame: 24 months
the mean endoscopic severity scores and the proportion of patients without ulcers
Time frame: after 24 months
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