RecruitingPhase 2NCT07333716

Desloratadine in Patients With Ulcerative Colitis

Efficacy and Safety of Desloratadine as Adjuvant Therapy in Patients With Ulcerative Colitis


Sponsor

Tanta University

Enrollment

44 participants

Start Date

Jan 26, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to investigate safety and therapeutic efficacy of antihistamine (desloratadine) on inflammation and disease activity when administered as adjuvant therapies with the traditional therapy 5-aminosalisylic acid (mesalamine) in patients with mild to moderate ulcerative colitis.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Inclusion Criteria4

  • Both male and female sex.
  • patients with age ranged from 18 to 65.
  • patients with active mild and moderate ulcerative colitis according to American College of Gastroenterology (ACG) Clinical Guideline.
  • Patients treated with 5-aminosalisylic acid (mesalamine).

Exclusion Criteria9

  • Patients with severe UC
  • Significant liver or kidney function abnormalities
  • Pregnant or lactating females
  • Treatment with systemic or rectal steroids
  • Treatment with immunosuppressant or biological therapies
  • Known allergy to desloratadine or any ingredient in the formulation
  • Patients with other inflammatory diseases
  • Patients with history of colon cancer
  • Patients with complete or partial colectomy

Interventions

DRUGDesloratadine

mesalamine 1000 mg three times daily plus desloratadine 5 mg once daily for 3 months.

DRUGmesalamine

mesalamine 1000 mg three times daily for 3 months


Locations(1)

Menofia university Hospitals

Shibīn al Kawm, Menofia, Egypt

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NCT07333716


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