Skip to content

Repeated Low-level Red Light for Myopia Progression Study: A 1-year, International, Multicenter, Multiethnic Randomized Controlled Trial

Repeated Low-level Red Light for Myopia Progression Study: A 1-year, International, Multicenter, Multiethnic Randomized Controlled Trial - An IPOSC Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000059598
Enrollment
30
Registered
2026-01-01
Start date
2026-01-01
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

Interventions

Subjects will be treated with a Myopia Management Devices (Eyerising International, South Yarra VIC, Australia) 5 days a week, three minutes per session, twice a day, with a minimum interval of 4 hour

Sponsors

Institute of Science Tokyo
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Age: 6 to 12 years at enrolment 2) Myopia: Cycloplegic SER -1.0 to -7.0 diopters (D) in each eye 3) Anisometropia : < 1.5 D 4) Astigmatism: < 1.5 D 5) Best corrected visual acuity (BCVA) 20/25 or better. 6) Informed parental consent

Exclusion criteria

Exclusion criteria: 1) Ophthalmic diseases, conditions, or syndromes other than ammetropia and myelinated nerve fiber layer, or prematurity (less than 36 weeks of gestation) 2) Previous use of optical or pharmacologic treatment for myopia control (e.g., defocusing spectacle or contact lenses, orthokeratology, atropine, or pirenzepine) 3) Systemic diseases (e.g., endocrine, cardiac diseases) and developmental anomalies 4) Inability to attend regular follow up visits

Design outcomes

Primary

MeasureTime frame
Changes in cycloplegic SER Changes in AL

Secondary

MeasureTime frame
Changes in the rate of SER and AL increase Changes in other biometric parameters except AL: ACD, CC, WTW, CT and choroidal structures. Best corrected visual acuity (BCVA), intraocular pressures, ocular and systemic symptoms, ocular signs assessed by slit lamp biomicroscopy and binocular indirect ophthalmoscopy, and questionnaire for self-reported visual function Pupil size in room light measured by pupillometer (option)

Countries

Japan,Asia(except Japan),North America

Contacts

Public ContactHiroyuki Takahashi

Institute of Science Tokyo Ophthalmology

t.hiroyuki.oph@tmd.ac.jp03-5803-5681

Outcome results

None listed

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