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Clinical Trial Summary

A Study to Evaluate the Safety and Efficacy of the Bausch + Lomb Myopia Control Lens for the Correction of Myopic Ametropia and Slowing the Progression of Myopia in Children


Clinical Trial Description

A Multi-center, Randomized, Parallel, Bilateral, Investigator-masked study to Evaluate the Safety and Efficacy of the Bausch + Lomb Myopia Control Lens for the Correction of Myopic Ametropia and Slowing the Progression of Myopia in Children ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06305663
Study type Interventional
Source Bausch & Lomb Incorporated
Contact Yan Zhang
Phone +86 21 60327166
Email Yan.Zhang1@bausch.com
Status Not yet recruiting
Phase N/A
Start date March 29, 2024
Completion date January 31, 2027

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