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Myopia Control Using Novel Soft Contact Lenses

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Recruitment opened Show 4 more changesShow less
    • Start date changed from estimate of Apr 16, 2026 to Aug 26, 2026
    • Study sites: 0 to 1
    • Eligibility criteria expanded, about 28 words
    • Secondary endpoints: details revised at 1 of 1 entry
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT07547085
Lead Sponsor The Hong Kong Polytechnic University
Collaborators: Eyebright Medical Technology (Beijing) Co., Ltd.
Conditions
(from sponsor)		 Myopia
Related terms Myopia
Enrollment 126 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov