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Randomized controlled trial for orthokeratology lens to correct anisomyopia in children

Randomized controlled trial for orthokeratology lens to correct anisomyopia in children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017535
Enrollment
Unknown
Registered
2018-08-02
Start date
2018-09-01
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

anisomyopia

Interventions

ortho-k group:overnight ortho-k wearing
spectacle group:full time single-vision spectacle wearing

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 14 Years

Inclusion criteria

Inclusion criteria: Aged 8 - 14 years; myopia of both eyes - 0.75 D to - 5.00 D; Cylinder =1.50D; The interocular difference in spherical equivalent=1.00D; The corrected visual acuity of both eyes = 4.9.

Exclusion criteria

Exclusion criteria: Wearing all kinds of contact lenses for more than 3 months. Suffering from eye diseases such as trichiasis, conjunctivitis, dry eye, incomplete eyelid closure, intermittent or dominant strabismus; Suffering from diabetes, asthma, low immunity and other general diseases; Systemic or local application of atropine and other drugs that may affect the development of ocular axial length; Those who are intolerant of corneal contact lenses or spectacles; Those who cannot insist on daily use of orthokeratology lenses or spectacles; Unwilling to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
axial length;spherical equivalent;

Countries

China

Contacts

Public ContactYueguo Chen

Peking University Third Hospital

chenyueguo@263.net+86 13701233876

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026