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Clinical Trials in the USA / NCT06884527
Active, not recruiting

Myopia Control With a Innovative Spectacle Lens - A Cessation Study

NCT06884527 · tracked via the Priya Life Science USA tracker
Sponsor
Essilor International
Phase
N/A
Started
2025-02-18
Last updated
2026-09-11

Condition(s) studied

Myopia Progressing

Investigational drug(s) / intervention(s)

Single Vision Lens to A innovative spectacle lensSingle Vision Lens to A innovative spectacle lens

Single Vision Lens to A innovative spectacle lens: Participants in this arm are from the test group of the previous clinical trial (NCT05174780), where they wore the innovative spectacle lenses for three years. They will now wear single vision lenses for 12 months.

Single Vision Lens to A innovative spectacle lens: Participants in this arm are from the control group of the previous clinical trial (NCT05174780), where they wore the single vision spectacle lenses for three years. They will now wear single vision lenses for another 12 months.

Study summary

The purpose of this study is to quantify myopic progression following cessation of a innovative spectacle lenses after 3 years' use.

Eligibility

Sex
ALL
Min age
9 Years
Max age
15 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Existing subjects from the NCT05174780 clinical study. * Ability to comply with study procedures. * Informed consent of parent/guardian and assent of subject. Exclusion Criteria: * Current ocular infection, inflammation, or irritation likely to affect vision.

Primary outcome measure(s)

Trial sites (5)

FacilityCityRegionStatus
Illinois College of Optometry Chicago Illinois
Kannarr Eye Care Pittsburg Kansas
New England College of Optometry Boston Massachusetts
SUNY College of Optometry New York New York
Sacco Eye Group Vestal New York
Official registry record

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 NCT06884527 on ClinicalTrials.gov ↗ ← All trials in the USA