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ABSTRACT: Purpose
To evaluate the efficacy and safety of the new defocus spectacle lens in preventing myopia progression compared with the conventional single-vision spectacle lens (SVL).Design
A randomized, open-label, controlled clinical trial.Subjects
Children aged 6 to 14 years with a cycloplegic spherical equivalent refraction (SER) of -1.00 to -3.50 diopters (D) in both eyes were enrolled.Methods
Eligible participants were randomly assigned in a 1:1 ratio to receive either the novel defocus spectacle lens (MYOGEN) or the SVL. Data from the right eyes at the 12-month follow-up were used for the current analysis.Main outcome measures
The primary outcome was the 1-year change in SER from baseline to 12 months. Secondary outcomes included changes in axial le
SUBMITTER: Han X
PROVIDER: S-EPMC12607012 | biostudies-literature | 2026 Jan
REPOSITORIES: biostudies-literature