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Study on the role of Vitamin D in patients wit Inflammatory Bowel Disease

Investigating the Role of Vitamin D in INFLAMMATORY BOWEL DISEASE: Exploring the Pathophysiological Insights,Immunomodulatory and anti inflammatory effects in a tertiary health centre of Uttar Pradesh - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/103074
Enrollment
102
Registered
2026-02-05
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K509- Crohns disease, unspecified

Interventions

Intervention1: Vitamin D: Vitamin D is given to all the participant patients having IBD and evaluated the vitamin D level periodically every 3 months up to 1 year of time Control Intervention1: Nil: N

Sponsors

Dr Mohamed Fiyas Konnola
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients diagnosed with Crohns disease or ulcerative colitis based on clinical, endoscopic histological or radiological findings Participants aged between 14 and 65 years regardless of disease activity who have been receiving treatment for at least six months Willingness to undergo serum vitamin D level assessment Patients with or without ongoing treatment for IBD Both active disease and remission phases can be included as per validated activity indices Written informed consent to participate in the study Willingness to comply with followup visits and further assessments as per study protocol

Exclusion criteria

Exclusion criteria: Patients with chronic illnesses or autoimmune diseases unrelated to IBD Current or recent use of high-dose vitamin D supplements or other medications affecting vitamin D metabolism Patients with primary bone disorders like osteoporosis or osteomalacia not related to IBD. Presence of significant liver disease, renal disease, or cardiovascular conditions that could confound results. Pregnant or lactating women due to altered vitamin D metabolism. Conditions unrelated to IBD that may cause malabsorption (e.g., celiac disease, short bowel syndrome). Patients who have undergone major gastrointestinal surgery in the past 3 months. Patients unable to comply with the study protocol, follow-up visits, or assessments. History of alcohol or substance abuse that could interfere with study participation or data accuracy.

Design outcomes

Primary

MeasureTime frame
Impact of Vitamin D supplementation on IBDTimepoint: Baseline,12 weeks,24 weeks

Secondary

MeasureTime frame
Adverse drug reaction of drugs Timepoint: Every two weeks for six weeks

Countries

India

Contacts

Public ContactDr Mohamed Fiyas Konnola

BRD medical college

talk2fiyas@hotmail.co.uk8089999846

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026