JPRN-UMIN000024336
Completed
未知
A study for the effects of ingestion of food containing plant extract and lutein on visual function.:A randomized, double-blind, placebo controlled trial - A study for the effects of ingestion of food containing plant extract and lutein on visual function.
TTC Co.,Ltd.0 sites110 target enrollmentMarch 1, 2017
ConditionsHealthy adult
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Healthy adult
- Sponsor
- TTC Co.,Ltd.
- Enrollment
- 110
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •(1\) Subjects who have amblyopia or strabismus. (2\) Subjects who are judged as presbyopia (the control width is less than 2\.5 D for dominant eye). (3\) Subjects who have an uncorrected serious refractive error for dominant eye. (4\) Subjects who have undergone ophthalmic surgery for dominant eye. (5\) Subjects who have a serious eye disease or history of eye disease. (6\) Subjects who have a disease (e.g., pollinosis) which may influence the outcome of the study (7\) Subjects who have been taking health foods containing plant hishi extract, lutein, vitamin E for 3 months or expected to use during study. (8\) Subjects who have been taking health foods or medicines which may have effects to the amplitude of accommodation (including eye fatigue) for 3 months or expected to use during study (9\) Subjects who have been taking health foods or medicines which may have effects to the stiffness of shoulder and neck for 3 months or expected to use during study (10\) Subjects who cannot execute a display work load test (11\) Subjects who may have allergy to the test foods (12\) Subjects who have under treatment or a history of serious disease(e.g., diabetes, liver disease, kidney disease, or heart disease) (13\) Subjects who have under treatment of drug addiction and/or alcoholism (14\) Subjects who are participating other clinical studies or went back from an agreement acquisition day and participated in other clinical studies within 3 months or who are planning to participate other clinical studies during this study (15\) Subjects who are pregnant, breastfeeding, or planning to be pregnant or breastfeeding during study (16\) Subjects who are judged as unsuitable by doctor for laboratory value, anthropometric measurements, or physical examination value (17\) Subjects who are judged as unsuitable for lifestyle questionnaire (18\) Subjects who are judged as unsuitable by doctor for other reasons.
Outcomes
Primary Outcomes
Not specified
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