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Effect of supplement on contrast sensitivity : a pilot study

Effect of supplement on contrast sensitivity : a pilot study - Effect of test supplement on contrast sensitivity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000033352
Enrollment
30
Registered
2018-07-13
Start date
2018-07-17
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

Ingestion of test supplement for 24 consecutive weeks

Sponsors

TTC Co.,Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Subjects aged from 45 to 65 years old (2) Subjects with low contrast sensitivity

Exclusion criteria

Exclusion criteria: (1) Subjects who have eye disease except refractive errors (e.g., Macular disease, optic media with advanced abnormalities) (2) Subject who are myopia over -6D (3) Subject who are daily corrected visual acuity less than 0.7 in both eyes (4) Subjects who are best corrected visual acuity of less than 1.0 (5)Subjects who have under treatment or a history of serious disease (e.g., diabetes, liver disease, kidney disease, or heart disease) (6)Subjects who have history of surgical resection of the gastrointestinal tract (except for appendectomy) (7) Subjects who routinely take lutein or zeaxanthin containing supplement within the past year (8) Subjects who have history of smoking within the past year (9) Subjects who routinely take medicine (including eye drops) or health foods that may affect the results of this study (10) Subjects who may have symptoms of hay fever during study period (11) Subjects having possibilities for emerging allergy related to the study (12) Subjects who are in long-term treatment (including medication, hospitalization, diet and exercise therapy )or are planning to take treatment during study period (13) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire (14) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on baseline examination (15) Subjects who intend to become pregnant or lactating (16) Subjects who have participated in other clinical study (17) Subjects who are judged as unsuitable by doctor for other reasons

Design outcomes

Primary

MeasureTime frame
Contrast sensitivity

Secondary

MeasureTime frame
Macular pigment optical density, Subjective symptom questionnaire, Visual acuity, Best corrected visual acuity, Serum lutein and zeaxanthin concentration

Countries

Japan

Contacts

Public ContactHiroyasu Shimada

TTC Co.,Ltd. Clinical Research Planning Department

h.shimada@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

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