LFR-260 vs Traditional Phoropter in Visual Acuity Testing

Status Completed

Clinical Trial Summary

The purpose of this study is to establish if LFR-260 (investigational device) is not inferior in effectiveness to a traditional phoropter (control device) when applied in visual acuity test in subjects undergoing a full routine eye examination. LFR-260 proposes to provide information of the visual capabilities of the patient. The test will be provided and supervised by a qualified eye care provider. The informed consent, screening, randomization (into the order of visual test device used), (visual) device testing (to include precision testing, remote and offsite testing) will all occur at a single visit.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05259163
Study type	Interventional
Source	Evolution Optiks Limited
Contact
Status	Completed
Phase	N/A
Start date	June 7, 2022
Completion date	January 6, 2023

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