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Longitudinal clinical study to evaluate ocular morphological changes associated with myopia in Japanese children

Longitudinal clinical study to evaluate myopic eyes of Japanese children - Longitudinal study of myopia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000053567
Enrollment
200
Registered
2024-02-13
Start date
2022-12-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myopia and myopic astigmatism

Interventions

None listed

Sponsors

Aichi Medical University
Lead Sponsor
University of Tokyo, University of Osaka
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - spherical power of subjective refraction is -4.00D ~ -0.50D - cylindrical power of subjective refraction is -1.50D ~ 0.00D - willing to come to the clinic for 2 years at least - willing to wear orthokeratology lenses or single-vision spectacle

Exclusion criteria

Exclusion criteria: - having any eye diseases except ametropia - having the history of any eye surgeries - having the history of any treatments for myopia control (orthokeratology, multi focal contact lenses or spectacles. atropine etc.) in last 6 month

Design outcomes

Primary

MeasureTime frame
Change of retinal structure with axial elongation in 2 years (If an additional consent from the patient can be obtained, the change will be evaluated from the third year onward as well. Consent will be obtained every two years.)

Secondary

MeasureTime frame
Change of corneal shape, corneal biomechanics, choroidal thickness and wavefront aberration with axial elongation in 2 years (If an additional consent from the patient can be obtained, the change will be evaluated from the third year onward as well. Consent will be obtained every two years.)

Countries

Japan

Contacts

Public ContactHikaru Asai

Aichi Medical University Myopia research course

h-hirata@menicon.co.jp0561-62-3311

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026