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Choroidal Response to Novel Spectacle Lens to Control Myopia Progression — CHERRY  

Myopia, Progressive Clinical Trial

Official title:
A Sub-Study to Assess the Choroidal Response to Novel Spectacle Lens to Control Myopia Progression (CHERRY)

Clinical Trial Summary

Diurnal variations in the thickness of the choroid have been reported in the literature, and, more recently, the role of the choroid has been studied with respect to its role in myopia (near-sightedness) progression.

Clinical Trial Description

Diurnal variations in the thickness of the choroid have been reported in the literature , and, more recently, the role of the choroid has been studied with respect to its role in myopia (near-sightedness) progression. SightGlass Vision, Inc is conducting a multi-site, randomized, controlled, interventional study to confirm the efficacy and safety of spectacle lenses designed to inhibit the progression of myopia by reducing image contrast in peripheral vision. CORE is participating as a clinical site in this three year study which aims to compare changes in ocular length and cycloplegic auto-refraction in children randomised to wear one of either two test or one control spectacle lens designs; the CPRO-1802-001 (Cypress_SG) study. The sponsor is interested in conducting choroidal thickness measurements only at CORE's site by inviting those participants who have already been found eligible for the CPRO-1802-001 study to participate in this parallel study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03818880
Study type Interventional
Source SightGlass Vision, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date December 18, 2018
Completion date May 1, 2024
View Details
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