Evaluation of Novel Spectacles Intended for Myopia Management in a Short-Term Study

Starting soon · Not applicable

Conditions studied: Myopia: Refractive Error

In brief

The primary objective of this study is to evaluate the visual acuity, wearability, and quality of vision with two novel multifocal glasses designs in habitual myopia control glasses wearers, in a non-dispensing study after short-term wear.

Key facts

Study ID

NCT07497672

Run by

Myoptechs, Inc

People needed

20

Starts

2026-04-15

Expected to finish

2026-12-15

Last updated by the study team

2026-04-01

Who can join

Age: 8 and older, up to 15. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 8 - 15 years of age, inclusive.
• Ability of the child to assent, and for one parent to provide permission to participate.
• Had an eye examination within the past year.
• Distance visual acuity of 20/25 (logMAR +0.10) or better in each eye with best corrected with sph/cyl subjective refraction.
• Habitual glasses wearer of either MiYOSMART or Stellest for at least 2 months. (Can also be a contact lens wearer but needs to wear either MiYOSMART or Stellest spectacles for a minimum of 6 hours on a typical day.)
• No history of binocular function anomaly (e.g., no history of strabismus), and no apparent strabismus.
• Good general health (defined by medication use that has not changed within the last month and the absence of medical conditions or treatments that are deemed confounding to the data, as determined by the investigator).

You may not qualify if…

• Current report of active ocular inflammation or infection.
• Astigmatism > 1.00 D in either eye
• History of previous eye surgery

Full record on ClinicalTrials.gov

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