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Investigateion of improvement of accommodation of eye for middle and old-aged adults : A randomized, double blinded, placebo controlled, and parallel group comparison study.

Investigateion of improvement of accommodation of eye for middle and old-aged adults : A randomized, double blinded, placebo controlled, and parallel group comparison study. - Effect of supplement on accommodation of eye.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000033448
Enrollment
110
Registered
2018-07-19
Start date
2018-07-19
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

imeQ co.Ltd
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age: 45 years or older, < 65 years old 2. Gender: Male or Female 3. Subjective eye fatigue 4. Have no eye diseases other than refractive error (near-sightedness, far-sightedness and astigmatism) 5. Cylinder eyesight (binocular vision) > 1.0. The specifications of eye-contact lens or glasses cannot be changed and replaced with new ones during the test period. 6. Written informed consent

Exclusion criteria

Exclusion criteria: 1. Conduct of lasik surgery during the past 6 months 2. Presence or history of hepatitis diseases or severe renal, endocrine, cardiovascular, gastric, lung, hematologic and metabolic disorder diseases 3. Risk of onset of pollen allergy during the study period (July to November) excluding the case that the disease starts from current year 4. Current medications (excluding on-demand use) 5. Any medications (including eye drop) for indication of eye strain or health foods intake 6. Presence or history of drug/food allergy 7. Receipt of investigational product in other clinical studies during the past one month or currently participating in other clinical studies 8. Female who is pregnant, breast-feeding or intends to become pregnant 9. Patients whom principal investigator judges inappropriate to invite to this study

Design outcomes

Primary

MeasureTime frame
Accommodation of eye 0 week, 4 weeks

Secondary

MeasureTime frame
Subjective symptoms (questionnaire)

Countries

Japan

Contacts

Public ContactNaomi Yuzawa

IMEQRD co.Ltd Sales Department

n-yuzawa@imeqrd.co.jp03-6205-6222

Outcome results

None listed

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