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Choroidal Response to the Modified Defocus Incorporated Multiple Segments Spectacle Lenses

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Notable Recruitment opened Show 4 more changesShow less
    • Study sites: 0 to 1
    • Start date changed from estimate of Apr 25, 2026 to Apr 24, 2026
    • Eligibility criteria expanded, about 20 words
    • Secondary endpoints: details revised at 2 of 2 entries
  2. Minor 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 short-term changes in choroidal thickness and efficacy of the study spectacle lenses in children. Participants will be prescribed with a pair of study spectacle lenses for daily use and visit the clinic once every week for the first month for checkup and tests. After the first month of follow-up, participants will visit at 1 month, 6- and 12-month for checkup. Choroidal thickness, axial length and refractive errors will be monitored.
Trial Details
NCT Number NCT07547072
Lead Sponsor The Hong Kong Polytechnic University
Collaborators: HOYA Lens Thailand LTD.
Conditions
(from sponsor)
Myopia
Related terms Myopia
Enrollment 108 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov