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Completed

NCT Number: NCT04761341

FLIO and the Influence of Oral Lutein Supplementation on Macular Pigment

To investigate the effects of lutein supplementation on macular pigment density using FLIO and MPOD measurements in patients with age-related macular degeneration and healthy subjects over a course of 6 months.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Department of Ophthalmology, Inselspital, Bern University Hostpital, University of Bern, Bern, Switzerland

Bern, 3010, Switzerland

About this study

The human macula is a small area of the retina responsible for central vision. The yellow macular pigment contains three carotenoids, lutein ((3R,3'R,6'R)-lutein), zeaxanthin ((3R,3'R)-zeaxanthin), and meso-zeaxanthin ((3R,3'S;meso)-zeaxanthin). The human body is unable to synthesize lutein and zeaxanthin, thus needs to be obtained from dietary sources such as green leafy vegetables and supplements. The function of the macular pigment is to act as a filter by absorbing blue light that may attenuate photochemical damage of the retina. Furthermore, it protects against light induced oxidative damage by functioning as an antioxidant; scavenging free radicals. A growing body of evidence has established a link between the concentrations of the macular pigment carotenoids, the macular pigment optical density (MPOD) levels, visual performance and the risk of macular degeneration.

The ability of the macular pigment to absorb or filter blue light can be measured as macular pigment optical density (MPOD), which is directly related to the quantity of lutein and zeaxanthin in the macula. Furthermore, preliminary data showed that macular pigment can be evaluated using Fluorescence lifetime imaging ophthalmoscopy (FLIO). In a previous study the investigators have shown that FLIO provides contrast for macular pigment in patients with AMD and healthy subjects.

The purpose of this study is to investigate the effects of oral lutein supplementation on macular pigment density using FLIO and MPOD measurements in healthy subjects and patients with age-related macular degeneration (AMD) over a course of 6 months. Furthermore, the investigators will assess whether compositional and functional alterations of the gut metagenome may be related to age-related macular degeneration, and the effects of lutein supplementation on the gut. In addition, to blood samples, stool samples will be analysed accordingly to the currently running study on "The role of the gut metagenome on the development of ophthalmic diseases" ClinicalTrials.gov Identifier: NCT02438111. Faecal analyses will provide insight to how oral lutein supplementation effects the gut microbiota and how it is influenced by serum lutein Levels.

Objective is to investigate the effects of lutein supplementation on macular pigment density using FLIO and MPOD measurements in patients with age-related macular degeneration and healthy subjects over a course of 6 months.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject must be willing to give written informed consent
  • Probands 18 years of age or greater
  • Both eyes will be assessed in the study

Exclusion criteria

  • Opacities of ocular media excluding detailed observation of the retina
  • Gastrointestinal diseases that could cause disturbance of dietary absorption
  • History of lutein supplementation
  • Allergy to lutein and zeaxanthin
  • Missing compliance

Treatment and study plan

NUTROF TOTAL

Drug

1 per day over a course of 3 months

Primary outcomes

  1. MPOD (macular pigment optical Density)

    Time frame: 6 Months

    Method to detect changes in macular pigment optic Density using dual wavelength autofluorescence

  2. Fluorescence Lifetime Imaging Ophthalmoscopy (FLIO)

    Time frame: 6 Months

    Retinal Autofluorescence lifetimes

  3. Macular pigment screener (MPS) II

    Time frame: 6 Months

    Screening Method to detect changes in macular pigment optic Density using heterochromatic flicker photometry

Secondary outcomes

  1. Contrast sensitivity

    Time frame: 6 Months

    Using Pelli-Robson charts

  2. Visual acuity

    Time frame: 6 Months

    Visual acuity using ETDRS charts

  3. Serum Lutein concentration

    Time frame: 6 Months

  4. Stool Analysis namely taxonomic and functional characterization of gut microbiota

    Time frame: 6 Months

Sponsors and collaborators

Lead sponsor

Insel Gruppe AG, University Hospital Bern

Other

Registry information

Acronym: FLOS

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Feb 18, 2021
Registry last updated
Jan 26, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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