Eye health study
Macular pigment density
up from day 30.
“Enhancement of Macular Pigment Optical Density and Contrast Sensitivity Following Supplementation with Supercritical Fluid Extraction-Based Lutein Ester Products: Evidence from a Randomized, Double-Blind, Placebo-Controlled Study in Healthy Adults.”To be published soon
Study design.
- Design
- Randomised, double-blind, placebo-controlled trial, three arms against placebo
- Participants
- 128 healthy adults aged 18 to 50 with a macular pigment optical density (MPOD) of 0.20 to 0.35
- Intervention
- Xanthogreen®, Xanthogreen® TOS or Xanthogreen® ULTRA, or placebo, for 90 days
- Measured
- MPOD by flicker photometry at 0.25°, 0.5° and 1° from the fovea on days 0, 15, 30, 60 and 90; secondary outcomes were contrast sensitivity, visual processing speed, intraocular pressure and dry eye symptoms
Key outcomes.
The results.
Significant from day 30 on all three grades. *p < 0.0001 vs placebo; TOS ahead of both other grades, p < 0.0001.
Significant from day 30 on all three grades. *p < 0.0001 vs placebo; TOS ahead of both other grades, p < 0.0001.
Significant from day 30 on all three grades. *p < 0.0001 vs placebo; TOS ahead of both other grades, p < 0.0001.
Significant from day 30 against placebo. *p < 0.0001, **p < 0.00001 vs placebo.
Also measured.
Visual processing speed, intraocular pressure and dry eye: no consistent treatment-specific effect was observed.
No clinically meaningful safety concerns: safe for use.
The publication.
“Enhancement of Macular Pigment Optical Density and Contrast Sensitivity Following Supplementation with Supercritical Fluid Extraction-Based Lutein Ester Products: Evidence from a Randomized, Double-Blind, Placebo-Controlled Study in Healthy Adults.” To be published soon.
Full text available on request.
These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.
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