RECRUITINGOBSERVATIONAL
Age-Related Macular Degeneration Benchmark Imaging Dataset (ABID)
About This Trial
1000 participants from up to 25 international locations who are at least 50 years old with either healthy eyes or a diagnosis of Age-Related Macular Degeneration (AMD) will be consented to provide images of their eyes for a new dataset. This dataset is an important step in developing an Artificial Intelligence (AI) based screening tool for AMD.
Who May Be Eligible (Plain English)
Who May Qualify:
- Participants greater than or equal to 50 years of age at time of signing willing to sign a consent form Form
- Willing to comply with all study procedures and sign the willing to sign a consent form Form (ICF)
- Individuals with normal healthy eyes or diagnosed with any stage of Age-Related Macular Degeneration (treatment naïve patients with early, intermediate, or late AMD). The diagnosis and eligibility review will be confirmed by Central Reading Center.
Who Should NOT Join This Trial:
- Therapeutic treatment for any type of AMD, in either eye. Supplements, such as AREDS2 formula, are allowed.
- Unable to acquire adequate quality images, as evaluated by the Central Reading Center
- Severe vision loss requiring urgent surgery
- Contraindicated for acquiring retinal images due to narrow anterior chamber angles or hypersensitivity to light
- A systemic or ocular condition that in the opinion of the Investigator would preclude participation in the study
- Unwilling to sign willing to sign a consent form form
- Currently or previously enrolled in an interventional AMD clinical trial
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
* Participants greater than or equal to 50 years of age at time of signing Informed Consent Form
* Willing to comply with all study procedures and sign the Informed Consent Form (ICF)
* Individuals with normal healthy eyes or diagnosed with any stage of Age-Related Macular Degeneration (treatment naïve patients with early, intermediate, or late AMD). The diagnosis and eligibility review will be confirmed by Central Reading Center.
Exclusion Criteria:
* Therapeutic treatment for any type of AMD, in either eye. Supplements, such as AREDS2 formula, are allowed.
* Unable to acquire adequate quality images, as evaluated by the Central Reading Center
* Severe vision loss requiring urgent surgery
* Contraindicated for acquiring retinal images due to narrow anterior chamber angles or hypersensitivity to light
* A systemic or ocular condition that in the opinion of the Investigator would preclude participation in the study
* Unwilling to sign informed consent form
* Currently or previously enrolled in an interventional AMD clinical trial
Treatments Being Tested
OTHER
Retinal Imaging
Eligible participants will undergo one retinal imaging session of both eyes for the following: * Single field stereo color fundus photography (cFP) - pre and post dilation * Macular spectral domain-optical coherence tomography (SD-OCT)
Locations (14)
Bergstrom Eye Research LLC
Fargo, North Dakota, United States
Erie Retina Research
Erie, Pennsylvania, United States
Retina Foundation of the Southwest
Dallas, Texas, United States
Valley Retina Institute
McAllen, Texas, United States
Retina Consultants of Texas (Houston)
The Woodlands, Texas, United States
University of Utah - John A. Moran Eye Center
Salt Lake City, Utah, United States
University Station Eye Care Clinic
Madison, Wisconsin, United States
Charles Research Center
Buenos Aires, Argentina
Adelaide Eye and Retina Centre
Adelaide, Australia
Centre Hospialier Intercommunal de Paradis (Centre Monticelli Paradis)
Marseille, France
University of Bonn - Department of Ophthalmology
Bonn, Germany
Sankara Nethralaya, Medical Research Foundation
Chennai, Tamil Nadu, India
Aravind Eye Hospital
Chennai, Tamil Nadu, India
Aga Khan University
Karachi, Pakistan