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Clinical Study of Myopia Control During Orthokeraotology

Clinical Study of Myopia Control During Orthokeraotology

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-RON-15007389
Enrollment
Unknown
Registered
2015-11-13
Start date
2014-09-30
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

Myopia

Interventions

1:wear orthokeratology lens
2:wear single focus spectacle

Sponsors

Eye Hostipal of WenZhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 14 Years

Inclusion criteria

Inclusion criteria: 1. aged 8~14 years old; 2. refractive errorspherical refraction -0.75~-6.00D, astigmatism with rule <= -1.50D.

Exclusion criteria

Exclusion criteria: 1. Evidence of amblyopia or strabismus; 2. History of ocular disease, surgery, or injury; 3. history of systemic disease or systemic medications with known ocular effects.

Design outcomes

Primary

MeasureTime frame
refraction;ocular biological parameters;choroidal thickness;Corneal biomechanics;

Secondary

MeasureTime frame
corneal thickness;height;weight;

Countries

China

Contacts

Public ContactLian Yan
alian745@hotmail.com+86 13957730045

Outcome results

None listed

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