OPTDR01 Feasibility for Automated Diabetic Retinopathy Detection
Completed
Conditions studied: Diabetic Retinopathy, Diabetes
In brief
In the United States, only 62% of the 37 million people with diabetes receive annual screening exams for diabetic retinopathy. One of the goals of the US Department of Health and Human Services Healthy People 2030 campaign is to increase diabetic retinopathy screening rates to 70.3%. Research indicates that low screening rates are associated with a variety of factors, including income levels, race and lack of access to care. Furthermore, because diabetic retinopathy frequently presents asymptomatically, non-adherence to screening results in postponed disease detection and a higher probability of vision loss. Currently, it is estimated that 9 million adults in the US are affected by diabetic retinopathy, and 1.8 million suffer from vision-threatening diabetic retinopathy. Importantly, the rates of vtDR vary greatly by race, with Hispanic individuals at 7.14% and Black individuals at 8.66%, compared to 3.55% in White individuals. Despite these alarming figures, the disease can be managed and vision loss can often be averted with early disease detection, thus highlighting the importance of increasing screening rates. A clear need exists for a diabetic retinopathy screening tool that can be deployed in primary care settings, addressing the shortage of specialist care and making screening more accessible to underserved populations. OPTDR01 will directly address these issues by providing accessible, high quality screening for diabetic retinopathy. OPTDR01 will automatically detect more than mild diabetic retinopathy (mtmDR) and vision-threatening diabetic retinopathy (vtDR) in diabetic adults who have not previously been diagnosed with mtmDR or vtDR.
Key facts
- Study ID
- NCT06343350
- Run by
- Optain Health
- People needed
- 300
- Starts
- 2024-04-01
- Expected to finish
- 2025-10-30
- Last updated by the study team
- 2026-02-27
Who can join
Age: 22 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Having met the criteria established by either the World Health Organization (WHO) or the American Diabetes Association (ADA):
- Age 22 or older
- Understand the study and volunteer to sign the informed consent
You may not qualify if…
- Unable to understand the study
- Unwilling to sign informed consent
- Indicate persistent vision loss, blurred vision, or floaters
- Previous diagnosis of macular edema, diabetic retinopathy (any level) proliferative retinopathy, radiation retinopathy, or retinal vein occlusion
- History of laser treatment of the retina or injections into either eye, or any history of retinal surgery
- Currently participating in another investigational eye study or actively receiving investigational product for diabetic retinopathy or diabetic macular edema
- A condition that, in the opinion of the investigator, would preclude participation in the study
- Contraindicated for imaging by fundus imaging systems used in the study because of hypersensitivity to light, recently underwent photodynamic therapy, or was taking medication that causes photosensitivity
- Known pregnancy
Where it is running
- Gastro SB — Chula Vista, California, United States
- Triwest Research Associates — San Diego, California, United States
- Gulf Coast Clinical Research — Houston, Texas, United States
Full record on ClinicalTrials.gov
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