Study on the improvement of ocular function by continuous ingestion of food

Not Applicable

• Conditions: Healthy subjects

• Registration Number: JPRN-UMIN000035920
• Lead Sponsor: HUMA R&D CORP

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-02-18
• Study Completion: 2019-06-14
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Not provided

Exclusion Criteria

1)Patients who are currently receiving any medication or outpatient treatment 2)Subjects currently undergoing exercise or diet therapy under the supervision of a physician. 3)Persons who are likely to develop allergies from test foods 4)People with pollinosis 5)Patients with current or past history of drug dependence or alcohol dependence 6)Patients who have been attending the hospital with psychiatric disorders (depression, etc.) or sleep disorders, or who have a history of psychiatric disorders in the past 7)Night or shift workers 8)Person who is extremely irregular in lifestyle such as eating and sleeping 9)Persons engaging in extreme prey 10)Patients with a current or past history of serious diseases such as diabetes mellitus, liver disease (hepatitis), renal disease, heart disease, etc., thyroid disease, adrenal disease, or other metabolic diseases. 11)Patients with ocular diseases other than refractive errors (hyperopia, myopia, astigmatism) 12)Persons with eyelashes extension 13)Persons who use health foods, supplements, and drugs that affect eye function. 14)Those who participated in another clinical study (study) within 3 months after the date of informed consent, or who are planned to participate in another clinical study (study) during the study period. 15)A blood sample exceeding 200 ml within 3 months or 400 ml within 3 months after the date of obtaining informed consent or a component blood donation. 16)Subjects who are currently pregnant or breast-feeding, or who may be pregnant or breastfeeding during the study period. 17)Current smokers or those who smoked within the past year 18)Persons who have difficulty complying with the records of various surveys 19)Subjects who are determined to be ineligible based on laboratory values and measurements at the time of SCR. 20)Other persons for whom the principal investigator judges to be inappropriate as subjects of the study.

Study & Design

• Study Type: Interventional
• Study Design: Not specified