We compare the effect of HyD (25-hydroxyvitamin D) and vitamin D3 in their effect on 25-hydroxyvitamin D plasma levels over a course of 4 month. This is a pharmacokinetic study including 35 postmenopausal women. * Trial with medicinal product
We include postmenopausal women age 50 to 75, race/ethnicity: Caucasian, serum 25(OH)D at baseline between 20 to 60 nmol/l, body mass index: \< 30 kg/m2 to compare 25(OH)D and vitamin D3 in equimolar doses over a 4 month pharmacokinetic trial. The dosing arms are daily, weekly, and bolus
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
35
daily (20ug), weekly (140 ug), Bolus (140 ug)
daily (800 IU), weekly (5600 IU), Bolus (5600 Iu)
University Hospital Zurich, Centre on Aging and Mobility
Zurich, Canton of Zurich, Switzerland
serum 25(OH)D levels
Time frame: repeated assessments over 4 months
muscle strength, blood pressure, blood glucose, bone markers
Time frame: repeated assessments over 4 months
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