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Dual Focus Soft Contact Lens Wear Cessation Study

Myopia Clinical Trial

Official title:
MiSight Lens Wear Cessation Study

Clinical Trial Summary

The purpose of this study is to investigate the effect of ceasing treatment with dual focus soft contact lenses.

Clinical Trial Description

This is a bilateral, open label, dispensing study with subjects who have completed dual focus soft contact lens wear treatment for either 3 or 6 years and who are refit to Proclear 1-day lens for 1 year. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05779072
Study type Interventional
Source Coopervision, Inc.
Contact
Status Completed
Phase N/A
Start date March 1, 2019
Completion date March 1, 2021
View Details
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