The aim of this study is to evaluate the bioavailability of "Novo C Plus" vitamin C containing dietary supplement compared to licensed vitamin C medications. The novelty of this product is the liposomal formulation.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
32
Ascorbic acid in different ways and doses
Semmelweis University - 1st Departement of Internal Medicine
Budapest, Hungary
Plasma ascorbic acid concentration area under curve
Plasma ascorbic acid concentration will be measured from peripheral blood samples after 30-45-60-90-120-180-240-300-360 minutes after getting the medication. Area under curve of time - plasma concentration curve will be calculated.
Time frame: 360 minutes
Safety and tolerability assessed by number of subjects with treatment-related adverse events as assessed by CTCAE v4.0
Time frame: 24 hours
Urine ascorbic acid excretion
Urine is collected for 12 hours after taking study drug, and urine ascorbic acid excretion will be calculated: urine ascorbic acod concentration (uM)×collected urine (L).
Time frame: 12 hours
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