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Myopia Control Using Novel Soft Contact Lenses

NCT07547085 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 126

Last updated 2026-04-23

No results posted yet for this study

Summary

The goal of this study is to investigate the myopic control efficacy of two study soft contact lenses in children. Participants will be prescribed Lens A, Lens B or single vision contact lenses for the first year. Participants in single vision contact lenses group will switch to Lens A at 12 months. All participants will then continue lens wear for an additional 12 months. Their cycloplegic refraction and axial length will be monitored every 6 months for 2 years.

Conditions

  • Myopia

Interventions

OTHER

Lens A

Lens A contact lens is a daily disposable silicon hydrogel contact lenses with peripheral myopic defocus.

OTHER

Lens B

Lens B contact lens is a daily disposable silicon hydrogel contact lenses with peripheral myopic defocus.

Sponsors & Collaborators

  • Eyebright Medical Technology (Beijing) Co., Ltd.

    collaborator INDUSTRY

  • The Hong Kong Polytechnic University

    lead OTHER

Principal Investigators

  • Rachel Ka Man Chun, PhD · School of Optometry, The Hong Kong Polytechnic University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
7 Years
Max Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-04-16
Primary Completion
2029-04-30
Completion
2029-07-14

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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 NCT07547085 on ClinicalTrials.gov