Absorption; Disorder Clinical Trial
Official title:
Randomized, Crossover, Double Blinded, Non-inferiority Study of Three Products Rich in Organic Silicon, in Postprandrial Situation
The objective of the present study is to evaluate the non-inferiority of the absorption parameters of three silicon supplements in human volunteers.
The objective of the present study is to evaluate the non-inferiority of the absorption
parameters of three silicon supplements in human volunteers.
Participants: 5 healthy men over 18 years old, with normal serum creatinine levels. Treatment
consists of one product consumption every week, and measuring postprandrial response at 0,
30, 60, 90, 120, 180, 240 and 360 min, in blood, and urine in two periods of three hours
each.
The statistical analysis will follow the principles specified in the guidelines of the ICHE
and CPMP/EWP/908/99 ICHE Points to Consider on Multiplicity Issues in Clinical Trials.
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