Effect of Lutein-enriched-egg Beverage on Age-Related Macular Degeneration (AMD)
NCT ID: NCT00902408
Last Updated: 2013-11-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
100 participants
INTERVENTIONAL
2009-07-31
2011-12-31
Brief Summary
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Detailed Description
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Objective: To assess whether there is the same increase in macular pigment optical density as in healthy subject and to see if there is any change in visual function after a year of intervention.
Study design: This will be a randomized, double blind, placebo controlled, interventional trial. Subjects will be randomized, stratified for gender and age, into two groups (N=50 each) receiving either the intervention product (base on 1.5 yolk of a lutein enriched egg containing 0.921 ± 0.106mg of lutein and 0.137 ± 0.014mg of zeaxanthin per yolk) or a placebo. Subject will be followed for 1 year and will be seen three times for measurements.
Study population: 100 subjects, ages 50 and older with drusen and/or Retinal pigment epithelium (RPE) alterations on retinal image.
Main study parameters/endpoints: Changes in amount of early macular degeneration signs on fundus photographs. Macular pigment optical density. Plasma lutein and zeaxanthin levels.
Nature and extend of the burden and risks associated with participation, benefit and group relatedness: Subjects will be seen three times with a total of 22 ( + 1 hour screening) hours. Methods used in this trial are commonly used techniques which have been proven safe in either previous trials or clinical practice. Subjects' sight will be limited for the investigated eye for a few hours after every visit because of the use of Tropicamide, this is standard practice at our ophthalmology department with only sporadic, and treatable side effects (acute angle-closure glaucoma in 0.03%). Subjects in the intervention group are expected to show a slower progression of the disease than those in the placebo group. We will be using the same egg-beverage as in the pilot study which showed no changes in lipid levels.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
QUADRUPLE
Study Groups
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Lutein
Lutein enriched eggs
Lutein enriched eggs
1 year of daily enriched lutein eggs or placebo
Placebo
Non enriched
Lutein enriched eggs
1 year of daily enriched lutein eggs or placebo
Interventions
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Lutein enriched eggs
1 year of daily enriched lutein eggs or placebo
Eligibility Criteria
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Inclusion Criteria
* 50 years and older
* Vision \> 0.5
* Non-smoker
* No ocular media opacity
* Uses no nutritional supplements containing Lutein or Zeaxanthin
* BMI \< 30
* No known cardiovascular disease
Exclusion Criteria
* Known lipid metabolism disease
* Blood lipid level modifiers (e.g. Statin)
* Known allergy to eggs or egg products
55 Years
85 Years
ALL
No
Sponsors
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Newtricious
UNKNOWN
Maastricht University Medical Center
OTHER
Responsible Party
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Principal Investigators
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Elton Kellly, MD
Role: PRINCIPAL_INVESTIGATOR
Maastricht University Medical Center
Locations
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University Eye Clinic Maastrich
Maastricht, Limburg, Netherlands
Countries
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References
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van der Made SM, Kelly ER, Berendschot TT, Kijlstra A, Lutjohann D, Plat J. Consuming a buttermilk drink containing lutein-enriched egg yolk daily for 1 year increased plasma lutein but did not affect serum lipid or lipoprotein concentrations in adults with early signs of age-related macular degeneration. J Nutr. 2014 Sep;144(9):1370-7. doi: 10.3945/jn.114.195503. Epub 2014 Jul 2.
Other Identifiers
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MEC 07-1-127
Identifier Type: -
Identifier Source: org_study_id