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

NCT07497672 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2026-04-01

No results posted yet for this study

Summary

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.

Conditions

  • Myopia: Refractive Error

Interventions

DEVICE

Habitual myopia glasses

Habitual myopia glasses of study P/905/25/MO

DEVICE

Myopia Glasses A

Myopia glasses A of study P/905/25/MO

DEVICE

Myopia Glasses B

Myopia glasses B of study P/905/25/MO

Sponsors & Collaborators

  • University of Waterloo School of Optometry and Vision Science

    collaborator UNKNOWN

  • Myoptechs, Inc

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
8 Years
Max Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-04-15
Primary Completion
2026-10-15
Completion
2026-12-15
FDA Device
Yes

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07497672 on ClinicalTrials.gov