Cholecalciferol in Chronic Inflammatory Bowel Diseases (5C)
IBD
About this trial
This is an interventional treatment trial for IBD
Eligibility Criteria
Inclusion Criteria: Confirmed IBD diagnosis; Age ≥ 18 years Exclusion Criteria: Hypercalcaemia defined as serum calcium value >2.70 mmol/l; Hyperparathyreoidism defined as serum iPTH value >65 ng/l; Hypoparathyreoidism defined as serum iPTH value <15 ng/l; Renal insufficiency defined as eGFR < 30 ml/min; Anamnesis of: Propensity to form calcium-containing kidney stones, Impaired renal calcium or phosphate excretion, Sarcoidosis; Pregnancy or lactation; Supplementation of vitamin D >200 IU/d (5μg/d) during study period; Administration of products that have a potential interaction with cholecalciferol, e.g. phenytoin, rifampicin, barbiturates, actinomycin, imidazole-antifungals
Sites / Locations
- Clarunis University Center for Gastrointestinal and Liver DiseasesRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
No Intervention
Weekly
Monthly
Control
weekly administration of one capsule, corresponding to approximately 3'500 IU cholecalciferol daily.
monthly administration of one capsule, corresponding to approximately 800 IU cholecalciferol daily.
no treatment