Assessment of DOT Spectacles in Chinese Children Extension
Condition(s) studied
Investigational drug(s) / intervention(s)
Novel spectacle lens design: Use of spectacle lenses may reduce the rate of progression of juvenile myopia
Study 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
Primary outcome measure(s)
- Axial length Group I — 12 months
Change in axial length from baseline to 36 months - Axial length Group II — 12 months
Change in axial length from baseline to 12 months
Trial sites (5)
| Facility | City | Region | Status |
|---|---|---|---|
| Aier Eye Hospital | Changsha | China | Recruiting |
| West China Hospital | Chengdu | China | Recruiting |
| Zhongshan Ophthalmic Center | Guangzhou | China | Not Yet Recruiting |
| Fudan University EENT | Shanghai | China | Recruiting |
| Tianjin Eye Hospital | Tianjin | China | Recruiting |
More SightGlass Vision, Inc. trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07008001 on ClinicalTrials.gov ↗ ← All trials in China