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Active Not RecruitingNCT04947735

CYPRESS Efficacy and Safety Study Extension

Control of Myopia Using Peripheral Diffusion Lenses: Efficacy and Safety Study Extension

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
SightGlass Vision, Inc. · Industry
Sex
All
Age
6 Years – 17 Years
Healthy volunteers
Accepted

Summary

This is an open-label, controlled, multisite, two-arm parallel group clinical trial of 36-month duration to evaluate the continued safety and efficacy of SightGlass Vision Diffusion Optics Technology (DOT) Spectacles in reducing the progression of juvenile myopia.

Conditions

Interventions

TypeNameDescription
DEVICENovel spectacle lens designUse of single vision, impact resistant spectacle lenses may reduce the rate of progression of juvenile myopia
DEVICESpectacle lensesSingle vision, impact resistant spectacle lenses

Timeline

Start date
2021-07-19
Primary completion
2025-04-30
Completion
2026-03-31
First posted
2021-07-01
Last updated
2024-12-20

Locations

12 sites across 2 countries: United States, Canada

Regulatory

Source: ClinicalTrials.gov record NCT04947735. Inclusion in this directory is not an endorsement.

CYPRESS Efficacy and Safety Study Extension (NCT04947735) · Clinical Trials Directory