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MiSight 1 Day Post-Approval Study for Effectiveness and Visual Symptoms

Myopia Clinical Trial

Official title:
MiSight 1 Day Post-Approval Study for Effectiveness and Visual Symptoms

Clinical Trial Summary

The purpose of this post-approval study is to confirm the effectiveness of the MiSight 1 Day lens in clinical practices within the US and to assess the stability of the myopia reduction over one-year post-treatment.

Clinical Trial Description

This study is a multicenter, parallel-group, controlled, double-masked (subject and investigator), randomized clinical trial with a total duration of four years. Part 1 of this study will study the effectiveness of MiSight 1 Day in slowing myopia progression over three years in a US population. Subjects in Part 1 will wear MiSight 1 Day lenses or Proclear 1 day lenses. Part 2 will study the stability of the effectiveness result over a one-year post-treatment period. All subjects in Part 2 will wear Proclear 1 day lenses. Subjects and investigators will remain masked from Part 1. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05285553
Study type Interventional
Source Coopervision, Inc.
Contact Kathryn Richdale, OD, PhD
Phone 917-755-4548
Email krichdale@coopervision.com
Status Recruiting
Phase N/A
Start date June 25, 2022
Completion date June 30, 2027
View Details
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