Evaluate the Possible Efficacy and Safety of Empagliflozin in Patient With Ulcerative Colitis
Ulcerative Colitis
About this trial
This is an interventional treatment trial for Ulcerative Colitis
Eligibility Criteria
Inclusion Criteria: •Patients with mild to moderate UC are diagnosed by history, clinical signs according to the Montreal classification of severity of ulcerative colitis and( Endoscopy, and biopsy) to establish the chronicity of inflammation and to exclude other causes of colitis. Exclusion Criteria: Other inflammatory bowel diseases (CD). History of serious hypersensitivity to empagliflozin or any component of the formulation. Patients on dialysis. Severe renal impairment (eGFR <20 ml/minute/1.73m2) . Chronic urinary tract infection. Chronic genital infection.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Placebo Comparator
Experimental
placebo group
empagliflozin group
Patients will receive conventional treatment only (corticosteroids +immune suppressive +amino salicylic acid) for 4 months.
Patients will receive conventional treatment (corticosteroids +immune suppressive + aminosalicylic acid) and empagliflozin (0.4 - 0.5mg/kg/day) orally (maximum dose 25mg per day)for 4months.