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Clinical Trial Summary

The objective of the present study is to evaluate the non-inferiority of the absorption parameters of three silicon supplements in human volunteers.


Clinical Trial Description

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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03108508
Study type Interventional
Source Technological Centre of Nutrition and Health, Spain
Contact
Status Completed
Phase N/A
Start date May 1, 2017
Completion date July 30, 2017

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