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Diabetic Retinopathy Tethered Augmented Reality With Eye4 Study — DRTARES  

Diabetic Retinopathy Clinical Trial

Official title:
Diabetic Retinopathy Tethered Augmented Reality With Eye4 Study

Clinical Trial Summary

Diabetes has reached epidemic levels in North America and with it, diabetic retinopathy is increasingly affecting the vision of millions of people. Despite treatment many patients still have vision loss that cannot be improved medically or with prescription eyeglasses. Our study is going to look at an FDA Class 1 Exempted visual aid that uses augmented reality to help people see better.

Clinical Trial Description

In this study subjects will have their best corrected visual acuity and contrast sensitivity compared to their best vision and contrast with the Eyedaptic device. The Eyedaptic device is an FDA 510(k) Class 1 Exempt device as it is a visual aid. This is a pilot study to determine whether subjects with diabetic retinopathy associated vision loss obtain a benefit with augmented reality vision. Subjects will receive a manifest refraction. When subjects have their optimal corrective lenses, the subjects' vision will be tested with their corrective lenses alone and again using the Eyedaptic device. This will be a single visit study, with no follow up. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05491746
Study type Interventional
Source Eyedaptic
Contact
Status Completed
Phase N/A
Start date July 1, 2022
Completion date October 1, 2022
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