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Clinical Trial Summary

This study was the evaluate the efficacy and safety of Spirulina maxima extract on the improvement of Cognitive Function


Clinical Trial Description

This study was 12 weeks, randomized, double-blind, placebo-controlled human trial to evaluate. 80 subjects participated in Spirulina maxima extract or placebo group. To evaluate the changes in the evaluation items when Spirulina maxima extract was taken 12 weeks compared with placebo. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04431843
Study type Interventional
Source Chonbuk National University Hospital
Contact
Status Completed
Phase N/A
Start date March 17, 2020
Completion date November 26, 2020

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