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NCT07333716RecruitingPhase 2

Desloratadine in Patients With Ulcerative Colitis

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

Source: ClinicalTrials.gov · Last updated 29 Jan 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
44 (estimated)
First submitted
1 Jan 2026
Start date
26 Jan 2026
Primary completion date
Feb 2027
Lead sponsor
Tanta University
NCT number
NCT07333716

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 44
  • From 26 Jan 2026 to the primary completion date, Feb 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Treatment with systemic or rectal steroids
  • Treatment with immunosuppressant or biological therapies

Other illness

  • Known allergy to desloratadine or any ingredient in the formulation
  • Patients with other inflammatory diseases
  • Patients with history of colon cancer

Other

  • Patients with severe UC
  • Significant liver or kidney function abnormalities
  • Pregnant or lactating females
  • Patients with complete or partial colectomy

Who the study is looking for

  • 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).

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Menofia university Hospitals
Coordinator of this site? Confirm its status
Shibīn al KawmEgyptRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.