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NCT05986136CompletedPhase 2/3

Dapagliflozin in Patients With Ulcerative Colitis

Clinical Study to Evaluate Safety and Efficacy of Dapagliflozin in Patients With Ulcerative Colitis

Source: ClinicalTrials.gov · Last updated 21 Sept 2026

Brief summary (registry, in English)

The inflammatory bowel diseases (IBD) are described as complex, recurrent inflammatory conditions which are manifested as Crohn's disease (CD) and ulcerative colitis (UC). The common symptoms of IBD include debilitating/severe diarrhea, abdominal pain, weight loss, and chronic fatigue; events that may culminate in life-threatening complications. The pathogenesis of IBD has been characterized as complex/multi-factorial that includes disruption of intestinal epithelial barrier with consequent translocation of commensal microbial products as the prime event that instigates severe immune responses and intestinal inflammation.

Status (registry)
Completed
Phase (registry)
Phase 2/3
Study type
Interventional
Enrollment
60 (actual)
First submitted
2 Aug 2023
Start date
20 Aug 2023
Primary completion date
20 Aug 2026
Lead sponsor
Mostafa Bahaa
NCT number
NCT05986136

What you commit to

  • Study type: Interventional · Phase 2/3
  • Participants enrolled: 60
  • From 20 Aug 2023 to the primary completion date, 20 Aug 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 taking immunosuppressives or biological therapies
  • Addiction to alcohol and / or drugs

Other illness

  • Colorectal cancer patients
  • Known allergy to the dapagliflozin

Other

  • Breast feeding
  • Significant liver and kidney function abnormalities
  • Patients with severe UC

Who the study is looking for

  • Age ≥ 18 years
  • Both male and female will be
  • Mild and moderate UC patients diagnosed and confirmed by endoscope

Age in the registry: 18 months to 60 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
Faculty of Medicine, Mansoura University
Coordinator of this site? Confirm its status
Al MansurahEgyptUnknown status

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