N/A
18 Years
65 Years
18 Years
65 Years
Open (Enrolling)
Both
Vitamin D Deficiency
Both
Vitamin D Deficiency
Trial Information
Inclusion Criteria:
Healthy volunteers . adults aged 18 - 65
Exclusion Criteria:
Intestinal malabsorption, lactose intolerance, medical illness (e.g. liver disease, kidney
disease, or diabetes), hypercalcemia, excessive alcohol use, pregnancy, use of
medications known to interfere with vitamin D metabolism e.g. anticonvulsants,
barbiturates, or steroids), granulomatous disease, use of vitamin D supplements, potential
for significant sun exposure (e.g., travel to a sunny vacation site or use of tanning
beds) within the month prior to, or during, the study. -
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Endpoint Classification: Bio-availability Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Prevention
Outcome Measure:
Serum 25(OH)D level
Outcome Time Frame:
0, 1 day, 7 days, 14 days
Safety Issue:
Yes
Authority:
Israel: Ministry of Health
Study ID:
No. 1-Version 1.
NCT ID:
NCT01807845
Start Date:
January 2013
Completion Date:
December 2013
Related Keywords:
- Vitamin D Deficiency
- Casein micelles
- vitamin D3 (cholecalciferol)
- Bioavailability
- Nanoencapsulation
- Nutrition
- Vitamin D Deficiency
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