An interventional study of Lutein-enriched-egg beverage (NWT-02) and Placebo in Age-related Macular Degeneration (AMD), sponsored by Newtricious R&D BV. Completed at 4 sites in 4 countries. Open to participants aged 50 Years and older. Per ClinicalTrials.gov, last updated 2016-09-21.
Sponsored by Newtricious R&D BV · Not applicable, Interventional, and Treatment
The purpose of the I-TEAM project is to assess whether there is a change in visual function and status of the retina after a year of intervention in subjects with early signs of Age-related Macular Degeneration.
1,474 studies on the registry are indexed under Macular Degeneration; 206 are open to participants now.
This study's enrollment of 120 is above the median of 51 across 985 interventional studies indexed under Macular Degeneration.
Browse Macular Degeneration studies →Newtricious R&D BV is the lead sponsor of 4 studies on the registry; none are open to participants now.
Counted across the registry records on this site, refreshed daily.
Early AMD (AREDS category 2)
OR
Intermediate AMD (AREDS category 3)
Exclusion Criteria:
Powder in sachets is provided and dissolved to prepare Lutein-enriched-egg beverage
Dietary Supplement: Lutein-enriched-egg beverage (NWT-02)
Powder in sachet to prepare beverage
Dietary Supplement: Placebo
Lutein, zeaxanthin and DHA-enriched-egg yolk combined with buttermilk beverage
color-, taste- and energy-matched powder without enriched egg-yolk
Visual function
Time frame: 12 months
Carotenoid levels
Levels of lutein and Zeaxanthin
Time frame: 12 months
This study is completed, as verified in Sep 2016. You cannot join it, but the record below documents what was studied.
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