Corn could be key to saving your eyesight
NCT ID NCT02113254
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether eating corn rich in zeaxanthin (a natural pigment) could increase the density of the macular pigment in the eye, which may help prevent age-related macular degeneration (AMD), a leading cause of blindness. Nine healthy volunteers aged 20-35 ate a daily serving of this corn for 10 weeks. The goal was to measure changes in macular pigment density and blood zeaxanthin levels.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- corn with high zeaxanthin content
- What this could lead to
- If it works, this could point toward a simple dietary strategy to help prevent age-related macular degeneration.
- What could go wrong
- This was a very small, early study with only 9 healthy volunteers, and it was terminated early. Results may not apply to older adults or those with the disease.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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9 people
The number who actually took part.
- Start date
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Feb 2014
- Finished
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Jun 2014
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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20 to 35 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: * Healthy volunteers, men and women * Corrected visual acuity upper or equal to 8/10 in two eyes. * Age: 20 - 35 years * Free and written consent signed by the participant and the investigator before any examination required by the research * Subject agreeing to be registered in the national file * Affiliated subject of a national insurance scheme Exclusion criteria: * Presence of AMD signs on one or two eyes * Histories of other evolutionary ocular pathologies susceptible to complicate the evaluation of the AMD and of the visual acuity (glaucoma, high myopia forte (\>= - 6 dioptres), strong retinopathy…) * Subject operated of de cataract * Lens Opacities (NO\>=3, et/ou NC\>=3, et/ou C\>=1 et/ou P\>=1 according to the LOCSII method) * Food complements in the year wich precedes (list of complements in appendix 2) * Hypersensitive people in the tropicamide, in the atropine, its by-products, or in one of the excipients of the tropicamide * Patients at risk of angle closure glaucoma * Body Masse Index \>= 30 kg/m2 * Current smoking or stop for less than 12 months * Diabetes * High blood pressure * Hyperlipidemia * Neuro-inflammatory diseases * Chronical gastro-intestinal diseases (Crohn …) * Taking of continuous medicine during more than one month, during the last 12 months (exception of the contraceptive pill) * Pregnant or breast-feeding woman * Vegetarian Patient * Participation in another clinical trial during 30 days wich precedes * Not compliant subjects * Subject without french national insurance scheme * Subject under guardianship judicial
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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CHU de Bordeaux
Bordeaux, 33000, France
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Other studies related to the condition(s) this trial covers.