Age-Related Eye Disease Study 2 (AREDS2) (AREDS2)
Age-related Macular Degeneration, Cataract
About this trial
This is an interventional treatment trial for Age-related Macular Degeneration focused on measuring age-related macular degeneration, AMD, lutein, zeaxanthin, docosahexaenoic acid, eicosapentaenoic acid
Eligibility Criteria
Inclusion Criteria: Men and women between the ages of 50 and 85 years Macular status ranges from large drusen in both eyes or large drusen in one eye and advanced AMD (neovascular AMD or geographic atrophy) in the fellow eye Exclusion Criteria: Ocular media not clear enough to allow good fundus photography
Sites / Locations
- University of Alabama at Birmingham
- Jones Eye Institute - UAMS
- Retina-Vitreous Associates Medical Group
- Shiley Eye Center - UCSD
- Loma Linda University
- Doheny Eye Institute
- Jules Stein Eye Institute
- VA Northern California Health Care System
- Southern California Desert Retina Consultants, MC
- University of California, Davis
- West Coast Retina Medical Group, Inc
- Pacific Eye Associates
- Colorado Retina Associates
- Eldorado Retina Associates, PC
- Yale University Eye Center
- Retina Group of Florida
- University of Florida
- Bascom Palmer Eye Institute
- Sarasota Retina Institute
- Center for Retina and Macular Disease
- Emory University Eye Center
- Georgia Retina, PC
- Northwestern University
- The University of Illinois
- NorthShore University HealthSystems
- Ingalls Memorial Hospital
- University of Iowa
- Retina Associates of Kentucky
- Paducah Retinal Center
- Elman Retina Group
- Wilmer Eye Institute, Johns Hopkins Hospital
- National Eye Institute
- The Retina Group of Washington
- Massachusetts Eye and Ear Infirmary
- Ophthalmic Consultants of Boston
- Kresge Eye Institute
- Henry Ford Health System - Eye Care Services
- Vision Research Foundation
- Vision Research Foundation
- Vision Research Foundation
- Mayo Clinic
- University Health Care - Mason Eye Institute
- Eye Foundation of Kansas City
- Mid-America Retina Consultants, PA
- The Retina Institute
- Washington University School of Medicine
- Delaware Valley Retina Associates
- UMDNJ
- Ophthalmic Consultants of Long Island
- New York Eye and Ear Infirmary
- Manhattan Eye, Ear and Throat Hospital
- University of Rochester Eye Institute
- Retina Consultants, PLLC
- The Research Foundation of SUNY/Stony Brook
- Western Carolina Retinal Associates
- UNC Department of Ophthalmology
- Charlotte Eye Ear Nose and Throat Associates
- Duke University
- Wake Forest University Eye Center
- Case Western Reserve University
- Retina Associates of Cleveland
- Ohio State University
- Retina Associates of Cleveland
- Retina Associates of Cleveland
- Dean McGee Eye Institute
- Devers Eye Institute
- Retina Northwest, PC
- Pennsylvania Retina Specialists, PC
- Penn State M.S. Hershey Medical Center
- Scheie Eye Institute
- Wills Eye Hospital/Mid Atlantic Retina
- Retina Vitreous Consultants
- University of Pittsburgh Medical Center
- Palmetto Retina Center
- Carolina Retina Center
- Southeastern Retina Associates, PC
- University of Tennessee
- Vanderbilt Eye Institute
- Texas Retina Associates
- Texas Retina Associates
- UT Southwestern Medical Center
- Baylor College of Medicine
- Retina Consultants of Houston
- Texas Retina Associates
- Scott and White Memorial Hospital
- John Moran Eye Center
- Fletcher Allen Health Care
- The Retina Group of Washington
- Retina Center Northwest
- University of Wisconsin
- The Medical College of Wisconsin
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Active Comparator
Active Comparator
Active Comparator
Placebo Comparator
Lutein/Zeaxanthin
DHA/EPA
Lutein/Zeaxanthin + DHA/EPA
Placebo/Control
lutein (10mg)/zeaxanthin (2 mg)
DHA (350 mg)/EPA (650 mg)
lutein (10 mg)/zeaxanthin (2 mg) + DHA (350 mg)/EPA (650 mg)
Considered control because all participants received the AREDS formulation