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NCT07269223Completed

Oral Vitamin D3 Effect on Inflammatory Biomarkers in Ulcerative Colitis Patients

Effect Of Oral Vitamin D3 Supplementation On Inflammatory Biomarkers In Patients With Ulcerative Colitis

Source: ClinicalTrials.gov · Last updated 27 Oct 2026

Brief summary (registry, in English)

This randomized controlled trial aims to evaluate the effect of oral vitamin D3 supplementation on inflammatory biomarkers and disease activity in Pakistani patients with moderate ulcerative colitis. Sixty patients will be randomized to receive either standard treatment alone/Placebo or standard treatment plus vitamin D3 (50,000 IU fortnightly) for 12 weeks. Primary outcomes include changes in blood (CRP, ESR, IL-6) and fecal (calprotectin) inflammatory biomarkers, and disease activity assessed by the partial Mayo score. Secondary outcomes include vitamin D status, dietary intake, and quality of life. The study will provide insights into the immune-modulating and anti-inflammatory role of vitamin D3 as an adjunct therapy in ulcerative colitis.

Status (registry)
Completed
Study type
Interventional
Enrollment
60 (actual)
First submitted
25 Nov 2025
Start date
2 Dec 2025
Primary completion date
15 Feb 2026
Lead sponsor
University of Veterinary and Animal Sciences, Lahore - Pakistan
NCT number
NCT07269223

What you commit to

  • Study type: Interventional
  • Participants enrolled: 60
  • From 2 Dec 2025 to the primary completion date, 15 Feb 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

  • Changes in the type and dosage of the drug during the study

Other illness

  • Patients suffering from Crohn's disease or any known autoimmune disease
  • Patients with known kidney disease
  • Patients with known liver disease

Other

  • Patients with mild and severe ulcerative colitis
  • Pregnant and lactating women

Who the study is looking for

  • • All patients diagnosed previously by standard clinical i.e Truelove and Witts and endoscopic/ colonoscopic criteria
    • Patients with moderate ulcerative colitis will be included
    • Both male and female patients will be included in the study
    • No change in the type and dosage of their medicine over the past month
    • Patient with severe vitamin D deficiency (\< 10 ng/mL) after screening
    • Patients who will provide written informed consent
    • Age: 20-40 year

Age in the registry: 20 years to 40 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
University of Veterinary & Animal Sciences, Lahore
Coordinator of this site? Confirm its status
LahorePakistanUnknown status

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