Skip to content

A multicenter retrospective cohort study observing the axial length control effects of a newly designed aspherical orthokeratology lens in myopic children under 12 years old.

A multicenter retrospective study observing the axial length control effects of a newly designed aspherical orthokeratology lens in myopic children under 12 years old

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400092491
Enrollment
Unknown
Registered
2024-11-18
Start date
2024-11-24
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Myopia

Interventions

Group 1 (Newly designed special aspherical orthokeratology lens) (eyes):none
Group 2 (Spherical orthokeratology lens designed by VST) (eyes):none
Group 3 (Aspherical orthokeratology lens designed by VST) (eyes):none

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Age: 8 to 12 years old, with no gender restriction. 2. Spherical power: -0.75D to -6.00D, with with-the-rule astigmatism = 1.0. 4. All participants are first-time wearers of orthokeratology lenses. 5. Daily wear of the orthokeratology lenses for 6 to 8 hours. 6. Continuous treatment with at least 1 year of follow-up. 7. No use of other myopia treatment methods that may interfere with the treatment results, such as combined use of atropine.

Exclusion criteria

Exclusion criteria: 1. Poor compliance, which may hinder the smooth progress of the study. 2. Presence of systemic diseases such as diabetes or hypertension that may cause ocular complications. 3. History of ocular surgery or other eye diseases. 4. Abnormal intraocular pressure. 5. Abnormal corneal endothelial cells. 6. If the subject shows severe lens decentration on topography examination one or two weeks after receiving the orthokeratology lenses, and has a pupil diameter greater than 4.7mm in bright conditions, or has low scores on subjective visual quality questionnaires and objective visual quality assessments. 7. Patients with keratoconus. 8. Other conditions deemed unsuitable for inclusion by the physician.

Design outcomes

Primary

MeasureTime frame
axial length;

Secondary

MeasureTime frame
equivalent spherical power;Kf, Ks;

Countries

China

Contacts

Public ContactHuibin Lv

Peking University Third Hospital

huibin_lv@163.com+86 134 6675 9982

Outcome results

None listed

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