The Vitamin D and Psoriasis Study
Recruiting
- Conditions
- Psoriasis vulgarisSkin - Dermatological conditionsDiet and Nutrition - Other diet and nutrition disordersHuman Genetics and Inherited Disorders - Other human genetics and inherited disorders
- Registration Number
- ACTRN12611000648921
- Lead Sponsor
- Massey University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Medically diagnosed psoriasis vulgaris
Exclusion Criteria
Smoking; chronic kidney or liver disease; currently taking vitamin D supplements, or have taken them within the past two months; pregnant or lactating, or planning to be in the near future; have commenced a new psoriasis treatment within the past three months and wish to continue
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in Psoriasis Area and Severity Index (PASI) scores in treatment group compared to placebo group.[Baseline, 3 months, 6 months, 9 months and 12 months.];Change in serum 25(OH)D levels and PASI scores according to different vitamin D receptor genetic polymorphisms.[Baseline, 3 months, 6 months, 9 months and 12 months.]
- Secondary Outcome Measures
Name Time Method Quality of life as assessed using the Dermatology Life Quality Index questionnaire.[Baseline, 3 months, 6 months, 9 months and 12 months.];Change in inflammatory marker levels in the treatment group compared to the placebo group.[Baseline, 3 months, 6 months, 9 months and 12 months.]