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NCT06335160Recruiting

Possible Efficacy and Safety of Mebendazole in Patients With Ulcerative Colitis Treated With Mesalamine

Clinical Study to Evaluate the Possible Efficacy and Safety of Mebendazole in Patients With Ulcerative Colitis Treated With Mesalamine

Source: ClinicalTrials.gov · Last updated 6 Feb 2026

Brief summary (registry, in English)

To evaluate the possible efficacy and safety of mebendazole in patients with ulcerative colitis treated with mesalamine

Status (registry)
Recruiting
Study type
Interventional
Enrollment
46 (estimated)
First submitted
21 Mar 2024
Start date
20 Apr 2024
Primary completion date
Apr 2026
Lead sponsor
Tanta University
NCT number
NCT06335160

What you commit to

  • Study type: Interventional
  • Planned participants: 46
  • From 20 Apr 2024 to the primary completion date, Apr 2026
  • 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

  • Patients taking rectal or systemic steroids
  • Patients on immunosuppressants or biological therapies
  • Addiction to alcohol and / or drugs
  • Patients receiving, metronidazole, warfarin, low dose of aspirin, clopidogril, enzyme inducers (phenytoin, carbamazepine) and inhibitors (valoproate) to avoid potential pharmacodynamics and pharmacokinetic interactions.

Other illness

  • Patients with Colorectal cancer patients
  • Known allergy to the studied medications
  • History of complete or partial colectomy.
  • Patients with congestive heart failure, other heart disease (arrhythmia, ischemic heart disease including angina and myocardial infarction).
  • Patients with other inflammatory diseases and active infection.
  • Patients with stressful condition (COPD, morbid obesity).
  • Patients with liver disease.
  • Patients with any type of seizures (case report for mebendazole induced convulsion).
  • Patients with renal disease (case report for mebendazole induced nephrotoxicity).
  • Patients with coagulation disorders.
  • Patients on metronidazole (to avoid Stevens-Johnson syndrome).
  • Patients with hypersensitivity to mebendazole, albendazole or benzimidazole

Other

  • \- Patients with severe UC
  • Significant liver and kidney function abnormalities
  • Diabetic patients
  • Patients with thrombocytopenia and neutropenia.
  • Patients using antioxidants.
  • Pregnant and lactating females.

Who the study is looking for

  • Age ≥ 18 years old Both male and female will be included Mild and moderate UC patients diagnosed and confirmed by endoscope Patient treated with 5-aminosalislic acid (mesalamine)

Age in the registry: 18 years to 75 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
Tanta Unuversity
Coordinator of this site? Confirm its status
TantaEgyptRecruiting

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