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NCT04225819Suspended

Adjunctive Treatment With Vitamin D3 in Patients With Active IBD

Adjunctive Treatment With Vitamin D3 in Patients With Active IBD (ACTIVATED): A Randomized, Double-blind, Placebo-controlled Trial

Source: ClinicalTrials.gov · Last updated 27 Apr 2026

Brief summary (registry, in English)

Inflammatory bowel disease ((IBD), which includes Crohn's disease (CD) and ulcerative colitis (UC)), is a chronic, immune-mediated disease characterized by recurrent episodes of relapse. The incidence of IBD is increasing worldwide and poses as a burden that reduces quality of life and has a significant impact on health care resources. The advent of monoclonal antibodies to tumor necrosis factor-α (anti-TNF) has revolutionized treatment of IBD, improving rates of remission and reducing hospitalizations and surgeries. Nevertheless, many patients do not adequately respond to these therapies or lose response over time. Thus, there is an important need for novel immunomodulating agents to improve our ability to achieve remission. Besides its traditional role in bone homeostasis, several studies have recognized the important role Vitamin D plays in modulating the immune response, cancer, and cardiovascular disease. Specifically, Vitamin D may mediate immunity by modulating autophagy in leukocytes and regulating the gut microbiome. Thus, Vitamin D may play an important role in IBD. Furthermore, evidence suggests that the effect of vitamin D may be mediated through the TNF-α pathway, suggesting a synergy with anti-TNF therapy. This is a randomized, double blind, placebo-controlled trial to study the effect of Vitamin D3 as an adjunct therapy for patients with active CD, UC, or IBD unspecified who are undergoing anti-TNF induction therapy.

Status (registry)
Suspended
Study type
Interventional
Enrollment
100 (estimated)
First submitted
3 Jan 2020
Start date
1 Oct 2020
Primary completion date
1 Apr 2028
Lead sponsor
Massachusetts General Hospital
NCT number
NCT04225819

Who cannot take part

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

Other illness

  • Known intolerance or hypersensitivity to oral vitamin D3 supplementation
  • Known celiac disease or subjects with a positive screen for celiac disease (elevated tissue transglutaminase antibodies)
  • History of hyperparathyroidism
  • History of renal calculi or chronic kidney disease
  • Evidence of untreated infection (e.g. Clostridium difficile)
  • History of chronic pancreatitis
  • History of cystic fibrosis
  • History of gastric bypass

Lab values

  • Serum calcium >11 mg/dL

Other

  • Inability to provide informed consent or unwilling or unlikely to comply with the requirements of the study.
  • Female subjects who are pregnant, lactating, or intending to become pregnant during the study period
  • Plasma 25(OH)D > 60 ng/mL
  • Initiation of anti-TNF treatment for extra-intestinal symptoms alone
  • Presence of stoma or J-pouch

Who the study is looking for

  • Established diagnosis of CD, UC, or IBD-unspecified
  • Initiating anti-TNF therapy for IBD within 2 weeks of baseline/randomization
  • Other non-anti-TNF IBD medications must remain stable during the treatment period with the exception of tapering of corticosteroids.
  • Recent (within 6 months) objective evidence of active IBD on colonoscopy along with elevated inflammatory markers (C-reactive protein >8 mg/L or fecal calprotectin >150 mcg/g)
  • Current disease activity defined as a Harvey Bradshaw index > 4 at baseline (week 0) for CD subjects or Simple Clinical Colitis Activity Index > 2 at baseline (week 0) for UC subjects.
  • Fecal Calprotectin level >150 mcg/g

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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Massachusetts General Hospital
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status

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