RecruitingNot ApplicableNCT07008001

Assessment of DOT Spectacles in Chinese Children Extension

Clinical Assessment of DOT Spectacle Lenses in Chinese Children Extension


Sponsor

SightGlass Vision, Inc.

Enrollment

175 participants

Start Date

Aug 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This is a randomized, controlled, open-label, evaluator-blinded, multicenter, clinical trial of 12-months duration to evaluate the continued safety and efficacy of Diffusion Optics Technology (DOT) spectacle lenses in reducing the progression of juvenile myopia in children of Chinese origin.


Eligibility

Min Age: 8 YearsMax Age: 16 Years

Inclusion Criteria4

  • Previously a successfully completed participant in the CATHAY study (NCT05562622)
  • Agree to wear the assigned spectacles constantly except for sleeping, swimming, or other activities in which spectacle wear would be dangerous or otherwise not possible (minimum of 10 hours per day)
  • Willingness to participate in the trial for 12 months without contact lens wear or any other myopia management intervention
  • The subject's parent(s) or legal guardian(s) must read, understand and sign the Statement of Informed Consent and receive a fully executed copy of the form

Exclusion Criteria1

  • \. Known allergy to proparacaine, tetracaine, or tropicamide or cyclopentolate

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Interventions

DEVICENovel spectacle lens design

Use of spectacle lenses may reduce the rate of progression of juvenile myopia


Locations(5)

Aier Eye Hospital

Changsha, China

West China Hospital

Chengdu, China

Zhongshan Ophthalmic Center

Guangzhou, China

Fudan University EENT

Shanghai, China

Tianjin Eye Hospital

Tianjin, China

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NCT07008001


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