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Study on the changes of ocular parameters after wearing orthokeratology

Study on the changes of ocular parameters after wearing orthokeratology

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOh-16008873
Enrollment
Unknown
Registered
2016-07-21
Start date
2016-08-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

ametropia

Interventions

The test was given to three groups according to different myopic diopters:wear orthokeratology lenses

Sponsors

The Eye Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 8 yrs and more; 2. Subject Refraction: -1.00D =Equal Sphere= -8.00D; 3. Best Correct Visual Acuity=0.8; 4. Intraocular pressures were all within normal limits (11~21mmHg).

Exclusion criteria

Exclusion criteria: 1. Ocular surface diseases and other eye diseases which can cause abnormalities of ocular surface; 2. Patients with histories of ocular injury or surgery or Orthokeratology treatment; 3. Abnormal ocular signs caused by systemic diseases; 4. Pathological changes of fundus; 5. Corneal staining and decentration of lens after wearing Ortho-k.

Design outcomes

Primary

MeasureTime frame
corneal thickness;choroidal thickness;—

Countries

China

Contacts

Public ContactJun Jiang

The Eye Hospital of Wenzhou Medical University

jjhsj@hotmail.com+86 13506511080

Outcome results

None listed

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