Comparing the effect of vitamin D weekly with daily in treatment of patients with vitamin D deficiency
Phase 4
- Conditions
- Vitamin D deficiency.Avitaminosis D
- Registration Number
- IRCT2017022022965N6
- Lead Sponsor
- Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 130
Inclusion Criteria
patients aged 18 years old and more
levels of 25 hydroxy vitamin D below 30 nmol per liter
Exclusion Criteria
Patient treated with vitamin D supplements during the past 3 months
pregnant women
lactating women
patients with cognitive and psychiatric disorders that are not able to attend and complete the study
patients who cannot receive oral medication
patients with hyper-calcaemia, hypo-calcaemia
patients with hyper-phosphatemia And Hypo-Phosphatemia
Patients with Advanced Liver Diseases
Patients with Renal Disease
Patients receiving drugs that affect serum levels of vitamin D (phenytoin, phenobarbital, carbamazepine, valproate, etc.)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Vitamin D deficiency. Timepoint: at baseline, at the end of study. Method of measurement: Blood sample.
- Secondary Outcome Measures
Name Time Method