K50.9 K51.9
Conditions
Interventions
Group 1: After informed consent, all patients will receive information material regarding vitamin D in the context of IBD. They will fill questionnaires regarding the history of their disease and curr
Sponsors
Universitätsklinikum Freiburg
Eligibility
Sex/Gender
All
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: - patients with confirmed diagnosis of IBD (Crohn's disease, ulcerative colitis, indeterminate colitis). - age >= 18 years
Exclusion criteria
Exclusion criteria: inability to consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| vitamin D serum concentration at baseline and after 6 (+/- 3 ) months | — |
Secondary
| Measure | Time frame |
|---|---|
| - IBD disease activity (as measured by Crohn's disease activity index [CDAI], Harvey Bradshaw index [HBI], colitis activity index [CAI]) as well as quality of life scores at baseline and during follow-up. - results of IBD-related blood tests collected at baseline and follow-up | — |
Countries
Germany
Contacts
Public ContactChristine Janssen
Universitätsklinikum FreiburgKlinik für Innere Medizin II
Outcome results
None listed