Myopia Clinical Trial - Kubota Glass Parameter Refinement Study

Status Not yet recruiting

Clinical Trial Summary

Length of the eye will be measured in subjects exposed to various stimulus characteristics using an electronic spectacle which presents illuminated targets to the eye. The results will be analyzed to determine which stimulus characteristics may be most beneficial for use in the device.

Clinical Trial Description

Axial length measurements will be taken before and after two-hour monocular exposure to various stimulus characteristics using an electronic spectacle which presents illuminated defocus targets to the retina. Areas of investigation include the dioptric amount of defocus, the intensity of illumination, the spectrum of illumination, and the shape of the illumination target. The transient axial length results will be analyzed to determine which stimulus characteristics may be most beneficial for slowing myopic eye growth. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06085430
Study type	Interventional
Source	Kubota Vision Inc.
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Status	Not yet recruiting
Phase	N/A
Start date	November 1, 2023
Completion date	May 30, 2024

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