Evaluation of vitamin D efficacy on biochemical markers
Phase 3
Recruiting
- Conditions
- Vitamin D Deficiency.
- Registration Number
- IRCT20101130005280N27
- Lead Sponsor
- ational Institute for Medical Research Development
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 280
Inclusion Criteria
aged between 18 to 65
having full consent for participation in trial
Exclusion Criteria
not taking any vitamin D supplement in the last three months before the trial
not having Chronic Liver Diseases, Cystic Fibrosis, Crohn's, and Sprue
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Bone Density. Timepoint: Baseline, 75th day. Method of measurement: BMD Method.;Anthropometric factors. Timepoint: Baseline, 75th day. Method of measurement: using standard scales for weight and height measurement.;Blood pressure. Timepoint: Baseline, 75th day. Method of measurement: Systolic and diastolic blood pressure measurement.;Depression. Timepoint: Baseline, 75th day. Method of measurement: Beck depression assessment.;Eating habits. Timepoint: baseline. Method of measurement: FFQ.;Biochemical state. Timepoint: Baseline, 75th day. Method of measurement: Blood test.
- Secondary Outcome Measures
Name Time Method