Geneva, Jan. 12 -- International Clinical Trials Registry received information related to the study (ChiCTR2500115755) titled 'Safety and Efficacy Study of Myopia Control Devices in Children and Adolescents' on Dec. 30, 2025.

Study Type: Interventional study

Study Design: Parallel

Primary Sponsor: Eye Hospital, Wenzhou Medical University

Condition: myopia

Intervention: experimental group:Wear defocused frame glasses (HOYA Xin Le Xue lenses)+myopia treatment device

Recruitment Status: Not Recruiting

Phase: 4

Date of First Enrollment: 2026-01-01

Target Sample Size: experimental group:65;control group:65;

Countries of Recruitment: China

To know more, visit https://www.chictr.org.cn/showproj.html?proj=301392

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