"Night Vision and Carotenoids"
Primary Purpose
Macular Degeneration
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
EyePromise Visual Edge
Sponsored by
About this trial
This is an interventional supportive care trial for Macular Degeneration focused on measuring Macular Disease
Eligibility Criteria
Inclusion Criteria:
- No significant supplementary carotenoids within last 10 weeks. Without significant media opacity, cataract or congenital / acquired retinal disease other than atrophic AMD or diabetic retinopathy. Minimum 20/25 to enroll.
Exclusion Criteria:
- Unwilling or medically / psychiatrically unable to take part in a 6 month study.
- Recent ophthalmologic surgery or treatment.
- Tricare, Retirees & Enlisted Navy Personnel excluded. Already taking an OTC product to improve their night vision (containing carotenoids, polyphenols like bilberry).
Sites / Locations
- The Captain James A. Lovell Federal Health Care Center (FHCC)
- Davis EyeCare
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Placebo
Active
Arm Description
Maltodextrin Placebo: Experimental is 1:2
Eye Promise Visual Edge containing 8 mg zeaxanthin & 4 mg lutein Placebo: Experimental is 1:2
Outcomes
Primary Outcome Measures
MPOD
1 degree macular pigment optic density
Secondary Outcome Measures
Vimetrics Central Vision Analyzer (CVA)
measure of contrast & glare
LuxIQ- preferred luminance
preferred luminance
Useful Field of Vision (UFOV) Brain HQ
eye-brain test of functional vision and vision attention
Full Information
NCT ID
NCT04741763
First Posted
January 13, 2021
Last Updated
February 3, 2021
Sponsor
Robert Davis
Collaborators
Davis EyeCare
1. Study Identification
Unique Protocol Identification Number
NCT04741763
Brief Title
"Night Vision and Carotenoids"
Official Title
"Night Vision and Carotenoids" A 2 Center Study of the Physiological Function of the Eyes
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
February 13, 2018 (Actual)
Primary Completion Date
August 20, 2019 (Actual)
Study Completion Date
August 20, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Robert Davis
Collaborators
Davis EyeCare
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Vision at twilight and night is more difficult and dangerous for the entire population, even more so for the elderly and especially for the elderly with degenerative disease. Multiple worldwide laboratories have demonstrated the ability to raise macular pigment optical density with dietary carotenoids. This proposal further evaluates the relationship between macular re- pigmentation and vision under stressed conditions simulating twilight and night driving.
Detailed Description
This is a study of the physiological function of the eyes at night. However, the risk of automobile injury or fatality (driver, passenger or pedestrian) associated with motor vehicle accidents has been determined to increase with age, as a result of the complex interplay of age-related declines in vision, motor and cognitive functioning. However, basic visual function is the foundation for higher order processing whether it is visual spatial or cognitive. Four recent studies reflect the cost of poor vision on driving. (www.visionimpactinstitute.org). For example, visual impairment among European drivers was examined in 2422 drivers from 5 European countries. Visual acuity, visual field, contrast sensitivity, glare sensitivity, and useful field of view were tested. Visual functions not included in the current licensing standards were found to be more impaired among drivers (compared to those functions legally required). Elderly drivers are particularly vulnerable to sensory visual impairment when driving at night, as they suffer declines in both Contrast sensitivity (CS), Glare Disability (GD) and Glare Recovery (GR).6
Justification for study involving humans
Carotenoid science is well developed with respect to the safe utilization of dietary lutein (L) /zeaxanthin (Zx) as studied by the National Institute of Health (NEI). The recently published NEI AREDS2 study- May 2013, further substantiated the safety and usefulness of prescribing the carotenoids (10 mg L / 2 mg Zx) in patients at high risk of AMD. 7 Significantly, the average American and veteran population are typically low dose consumer of these carotenoids (1 to 2 mg/day for the average American).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Macular Degeneration
Keywords
Macular Disease
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Capsule type that results in null or increased MPOD (macular pigment optical density in du -density units) - either Maltodextrin Placebo or OTC commercial "Night Vision Formulation" consisting of 21 mg carotenoid capsule (14 mg zeaxanthin and 7mg lutein) supplied by www.zeavision.com (Chesterfield, MO) in research coded bottles with code held by the company. Gel caps will be supplied in a single 180 count bottle. 1 gel cap per day will be taken with a meal. Subjects will be called by telephone to improve compliance. Supplement compliance will ultimately be gauged by the number of tablets returned.
Masking
ParticipantCare ProviderInvestigator
Masking Description
Research coded bottles with code held by the sponsor. Gel caps will be supplied in a single 180 count bottle. 1 gel cap per day will be taken with a meal.
Allocation
Randomized
Enrollment
27 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Maltodextrin Placebo: Experimental is 1:2
Arm Title
Active
Arm Type
Experimental
Arm Description
Eye Promise Visual Edge containing 8 mg zeaxanthin & 4 mg lutein Placebo: Experimental is 1:2
Intervention Type
Dietary Supplement
Intervention Name(s)
EyePromise Visual Edge
Intervention Description
A dietary eye supplement containing 8 mg zeaxanthin and 4 mg lutein and additional proprietary nutrients
Primary Outcome Measure Information:
Title
MPOD
Description
1 degree macular pigment optic density
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
Vimetrics Central Vision Analyzer (CVA)
Description
measure of contrast & glare
Time Frame
24 weeks
Title
LuxIQ- preferred luminance
Description
preferred luminance
Time Frame
24 weeks
Title
Useful Field of Vision (UFOV) Brain HQ
Description
eye-brain test of functional vision and vision attention
Time Frame
24 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
No significant supplementary carotenoids within last 10 weeks. Without significant media opacity, cataract or congenital / acquired retinal disease other than atrophic AMD or diabetic retinopathy. Minimum 20/25 to enroll.
Exclusion Criteria:
Unwilling or medically / psychiatrically unable to take part in a 6 month study.
Recent ophthalmologic surgery or treatment.
Tricare, Retirees & Enlisted Navy Personnel excluded. Already taking an OTC product to improve their night vision (containing carotenoids, polyphenols like bilberry).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven Novil, PhD, ND
Organizational Affiliation
Optometry Research Lab manager, Optometry Clinic- Captain James A Lovell FHCC
Official's Role
Study Director
Facility Information:
Facility Name
The Captain James A. Lovell Federal Health Care Center (FHCC)
City
North Chicago
State/Province
Illinois
ZIP/Postal Code
60064
Country
United States
Facility Name
Davis EyeCare
City
Oak Lawn
State/Province
Illinois
ZIP/Postal Code
60453
Country
United States
12. IPD Sharing Statement
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"Night Vision and Carotenoids"
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