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)
View Full Details on ClinicalTrials.gov
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NCT07008001
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