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Myopia control by using an extended depth of focus contact lens

Myopia control by using an extended depth of focus contact lens

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs052200102
Enrollment
100
Registered
2020-12-22
Start date
2020-12-22
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 Myopia

Interventions

Contact lens wear

Sponsors

Koh Shizuka
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.6 to 12 years old when obtaining consent 2.Refractive error between -1.00 D and -6.00 D, astigmatism equal or less than 0.75D 3.The difference in spherical equivalent of the subjective refraction between both eyes is less than 1.00 D 4.Those with corrected vision of 0.8 or more in both eyes 5.Those who can consult for regular inspection 6.Those who have given written consent by voluntary will

Exclusion criteria

Exclusion criteria: 1.Obvious abnormal eye position or overt strabismus 2.Having ocular disease that affects contact lens wear 3.Having systemic disease 4.Previous history of ocular surgery 5.Use of drugs, eye drops or supplements that would affect accommodative function 6.Receiving myopia progression prevention treatment such as bifocal glasses, multifocal contact lens, orthokeratology lens, drug treatment within 3 months 7.Judged to be inappropriate for the study subject

Design outcomes

Primary

MeasureTime frame
Changes in axial length under accommodative paralysis between the baseline visit and last visit 12-month visit

Secondary

MeasureTime frame
1. Changes in axial length under accommodative paralysis between the baseline visit and last visit 6-month visit 2. Changes in refraction under accommodative paralysis between the baseline visit and last visit 12-month visit 3. Visual performance at every examination visit 4. Adverse events which are observed between the baseline visit and 12-month visit and considered as those associated with of devices used in the study 5. Contrast sensitivity, ocular higher-order aberrations for 4-mm and 6-mm pupil, and axial length under accommodative paralysis

Contacts

Public ContactShizuka Koh

Osaka University Hospital

skoh@ophthal.med.osaka-u.ac.jp+81-6-6879-5111

Outcome results

None listed

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