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Clinical Trial Summary

Randomized, controlled, multisite, subject-and observer-masked, 3-arm parallel group clinical trial of 36-month duration to evaluate the safety and efficacy of a novel spectacle lens design in reducing the progression of juvenile myopia.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03623074
Study type Interventional
Source SightGlass Vision, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date July 16, 2018
Completion date June 30, 2024

See also
  Status Clinical Trial Phase
Recruiting NCT06034327 - Efficacy in Controlling Myopia in Young Children Using a Novel Spectacle Lens N/A
Active, not recruiting NCT05893979 - Myopia Control Spectacle Lens Cessation Study N/A
Active, not recruiting NCT04947735 - CYPRESS Efficacy and Safety Study Extension N/A
Active, not recruiting NCT05617794 - Effect of Diffusion Optics Technology (DOT) Spectacle Lenses on Choroidal Thickness N/A
Active, not recruiting NCT05562622 - Assessment of DOT Spectacles in Chinese Children N/A
Completed NCT05650190 - Spectacle Lens Visual Acuity Assessments Study N/A
Completed NCT04126057 - Myopia Assessment of Two Manufacturing Processes N/A