Investigation of the effect of ingestion of test foods on cognitive function - Investigation of the effect of ingestion of test foods on cognitive function

HUMA R&D CORP0 sites16 target enrollmentAugust 27, 2018

Overview

Phase: 未知
Intervention: Not specified
Conditions: Not specified
Sponsor: HUMA R&D CORP
Enrollment: 16
Status: Completed
Last Updated: 2 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

No summary available.

Registry

who.int

Start Date

August 27, 2018

End Date

November 12, 2018

Last Updated

2 years ago

Study Type

Interventional

Sex

All

Investigators

Sponsor

HUMA R&D CORP

Eligibility Criteria

Inclusion Criteria

Not provided

Exclusion Criteria

•1\)A person who is currently receiving any drug treatment or ambulatory treatment. 2\)A person who is currently engaged in exercise or diet therapy under the supervision of a physician. 3\)Persons with a history or present disease or complication of liver disease or serious renal, endocrine, cardiovascular, gastrointestinal, pulmonary, hematologic, or metabolic diseases 4\)Persons with a history of drug or food allergy 5\)Persons who wish to do so during pregnancy, lactation, or the study period 6\)Persons with serious brain disease or a history 7\)Persons who have received blood donations or vaccinations within the last 3 months or who may receive them during the study period. 8\)Persons who routinely consume health foods, supplements, and pharmaceuticals that affect cognitive function 9\)Persons with psychiatric disorder (depression, etc.) or sleep disorder, etc. who have visited the hospital or have previously visited the psychiatric department. 10\)Alcohol\-dependent, drug\-dependent, or drug\-abused persons who are being treated or have a history of such treatment 11\)Persons who work on a shift basis, such as those who work at night 12\)Those who eat extremely biased meals 13\)Persons with extremely irregular lifestyle habits such as diet and sleep 14\)Individuals who have participated in other clinical trials (studies) within 3 months from the date of informed consent, or who plan to participate in other clinical trials (studies) during the course of this study 15\)Persons with difficulties in observing records on various questionnaires 16\)Other persons who are judged by the investigator to be inappropriate for the study.