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A study evaluating the effect of botanical ingredient-containing food on eye strain.

A study evaluating the effect of botanical ingredient-containing food on eye strain. - A study evaluating the efficacy of botanical ingredient-containing food on eye strain.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000034224
Enrollment
30
Registered
2018-10-30
Start date
2017-11-10
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy adults

Interventions

Sponsors

Kirin company
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Individuals aged from 20 to 65 years, when giving the informed consent. (2)Individuals who are aware of eye strain. (3)Individuals giving the written informed consent.

Exclusion criteria

Exclusion criteria: (1)Individuals who use medication or supplements or functional foods affecting eye strain. (2)Individuals who is not suitable for subjects by pre-test questionnaire. (3)Individuals who declare the allergy symptoms against test diets. (4)Individuals who have a chronic disease and use medicines continuously, or have a history of chronic disease. (5)Individuals who have a history of serious disease (e.g., diabetes, liver disease, kidney disease, and/or heart disease), thyroid gland disease, adrenal gland disease, and/or metabolic disorder, or have a history of these disease. (6)Individuals who have a history of digestive disease affecting digestion and absorption. (7)Individuals who have ophthalmologic disease, or have a history of ophthalmologic disease. (8)Individuals who is not suitable for subjects by pre-test. (9)Individuals who are planned to participate in other clinical study. (10)Individuals who have donated over 200 mL of blood and/or blood component within the last one month prior to the current study or over 400 mL of blood and/or blood component within the last three months prior to the current study. (11)Individuals with excessive alcohol-drinking behaviors. (12)Individuals who can't stop drinking for the days before the pre-check day and check days. (13)Individuals who have under treatment or a history of drug addiction and/or alcoholism. (14)Individuals who are planned to become pregnant after informed consent for the current study or are pregnant or lactating. (15)Individuals who are judged as unsuitable for the study by the investigator for other reason.

Design outcomes

Primary

MeasureTime frame
High Frequency Component 1

Secondary

MeasureTime frame
Visual Analogue Scale questionnaire

Countries

Japan

Contacts

Public ContactMasao Matsuoka

HUMA R&D CORP Clinical Development Division

matsuoka@huma-c.co.jp03-3431-1260

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026