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Not Yet Recruiting NCT05626166

the Efficacy and Safety of Diosmin in Patients With Ulcerative Colitis

Conditions: Ulcerative Colitis

Sex: All
Ages: 18 Years – N/A
Phase: PHASE3
Enrollment: 60
Sponsor: Tanta University

Summary

This is a randomized, controlled study evaluating diosmin tablets administered daily for 3 months. The purpose of the study is to evaluate the efficacy and safety of diosmin in the treatment of mild to moderately active ulcerative colitis. Disease activity will be measured using modified truelove and witt's classification.

Eligibility Criteria

Inclusion Criteria:Age ≥18 years old.Both male and female sex.Newly diagnosed patients with mild and moderate ulcerative colitis and treated with 5-aminosalicylic acid (mesalamine).Exclusion Criteria:Patients with severe ulcerative colitis.Patients with colorectal cancer.Patients on rectal or systemic steroids.Patients on immunosuppressants or biological therapies.Patients with previously failed treatment with sulphasalazine.Patients with known allergy to study medications.History of complete or partial colectomy.Patients with heart diseases and arrhythmia.Patients on blood thinning agents.Patients on anticoagulants (warfarin), anticonvulsants (carbamazepine and phenytoin), muscle relaxants (chlorzoxazone) and non-steroidal anti-inflammatory drugs (diclofenac).

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05626166). StuddyBuddy aggregates publicly available trial information.