Behcet's disease. Behçet disease
Conditions
Interventions
Intervention 1: The treatment group will receive vitamin D soft gel (D-VITIN, Zahravi) containing 50000 units of cholecalciferol [(3ß,5Z,7E)-9,10-secocholesta-
5,7,10(19)-trien-3-ol] one soft gel oral
Treatment - Drugs
The treatment group will receive vitamin D soft gel (D-VITIN, Zahravi) containing 50000 units of cholecalciferol [(3ß,5Z,7E)-9,10-secocholesta-
5,7,10(19)-trien-3-ol] one soft gel orally after meal e
The control group will receive one soft gel containing placebo orally after meal every 2 weeks for 6 months.
Sponsors
Vice chancellor for research, Tabriz University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Inclusion criteria: 1. Having active Behcet’s disease: Iranian Behcet's Disease Dynamic Activity Measure (IBDDAM) more than 2.5 Exclusion criteria: 1. Consumption of vitamin D supplements in the past 6 months 2. Pregnancy 3. Malabsorption 4. Renal failure 5. Hepatic failure
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Behcet's disease activity. Timepoint: Before intervention, 3 and 6 months after intervention. Method of measurement: Iranian Behcet’s Disease Dynamic Activity Measure questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Complications of vitamin D supplementation. Timepoint: 3 and 6 months after the intervention. Method of measurement: History and physical examination. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMehrzad Hajiallilo
Tabriz University of Medical Sciences
Outcome results
None listed