United Medical Research Institute
Inglewood, California, 90301, United States
NCT Number: NCT03929588
Single-center, open-label, prospective study in healthy volunteers desiring refraction for correction of visual acuity to compare a handheld device supported by a mobile application with the phoropter and autorefractor.
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Notify Me30 year–65 year
All sexes
Interventional
Not applicable
Inglewood, California, 90301, United States
Single-center, open-label, prospective study in healthy volunteers desiring refraction for correction of visual acuity to compare a handheld device supported by a mobile application with the phoropter and autorefractor in male or female subjects 30 to 65 years of age.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Hand-held device supported by a mobile application to obtain refractive error of the eye.
Manual refraction and ETDRS chart
Automated refraction
Time frame: Through study completion, an average of 5 months
Best-corrected visual acuity (BVCA) utilizing refraction results using the handheld device with supporting application will be compared to standard manual refraction methods (using a phoropter) for the age stratum 45 through 65 years.
EyeQue Corp.
Industry
A Clinical Validation Study to Evaluate the Performance of a Hand-held Device Supported by a Mobile Application Compared With Standard Eye Care Diagnostic Devices in Measuring Refractive Error of the Eye
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