Myopia Clinical Trial - MiSight 1 Day Safety Post-Approval Study

Status Recruiting

Clinical Trial Summary

The purpose of this post-approval study is to confirm the safety of daily disposable soft contact lens wear among the intended patient population for the MiSight 1 Day lens in the US.

Clinical Trial Description

This prospective post-approval study of safety in a US study population is to confirm the safety of MiSight 1 day lenses. Consecutive subjects receiving the MiSight 1 Day lens, who meet the inclusion criteria, will be prospectively offered to participate in the study. Additionally, safety data from the MiSight 1 Day Post-Approval Study for Effectiveness and Visual Symptoms (PAS001) will be used to supplement this safety study. ;

Study Design

Related Conditions & MeSH terms

Myopia

Clinical Trial Details

NCT number	NCT05285527
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	August 15, 2022
Completion date	May 30, 2027

View Details

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