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Clinical trial on the use of outdoor environment glasses for a suppressive effect on myopia progression

Clinical trial on the use of outdoor environment glasses for a suppressive effect on myopia progression - Clinical trial on the use of outdoor environment glasses for a suppressive effect on myopia progression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000023386
Enrollment
140
Registered
2016-07-29
Start date
2016-07-20
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 in school children

Interventions

Wearing outdoor environment glasses Wearing normal glasses

Sponsors

Hara Eye Clinic, Hakuyukai, Medical Corporation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Male and female school children between 6 and 12 years of age (elementary school 1st to 6th grade) at the time of obtaining informed consent (2) School children who spend at least 1 hour every day outside (3) School children with paralysis* of accommodation in both eyes where the objective spherical equivalent of each is between -1.50D and 4.50D (4) School children with at least one parent who has myopia (5) School children who can wear glasses daily and attend the clinic for consultations in accordance with the protocol (6) School children who do not have eye diseases other than refractive error (7) School children who have provided written informed consent themselves and written informed consent has been obtained from their parental authority for participation in this study

Exclusion criteria

Exclusion criteria: (1) School children with a history of wearing bifocal or progressive power lenses (2) School children with a history of wearing orthokeratology lenses (3) School children with unequal parallax exceeding 1.50D (4) School children with astigmatism exceeding 1.50D (5) School children with overt strabismus (6) School children who have received refractive surgery in the past (7) School children with keratoconus or herpes conjunctivitis, papillary proliferation, etc. (8) School children who are participating in other similar clinical research (9) School children who are judged to be inappropriate as subjects for this study by the principle investigator (or investigator) for the study (in charge)

Design outcomes

Primary

MeasureTime frame
Change in axial length between observation at baseline and observation after 24 months

Countries

Japan

Contacts

Public ContactTomomi Okano

Satt Co., Ltd. Clinical Research Group

myopia@sa-tt.co.jp03-5312-5026

Outcome results

None listed

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