Peripheral Optics in Myopia and Orthokeratology

The Hong Kong Polytechnic University

Status: Completed

Conditions: Myopia

Treatments: Device: Orthokeratology lenses; Device: Spectacles

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT00978679

G-RGVM

Details and patient eligibility

About

The primary objective of the current study is to investigate changes in peripheral refraction and aberration in children wearing orthokeratology lenses and single-vision spectacles.

Full description

Apart from being effective in reducing low to moderate myopia, orthokeratology has been shown to have potential in retarding myopic progression. The central cornea is flattened and peripheral optics altered in orthokeratology and it has been suggested that orthokeratology slows myopic progression through the alteration of peripheral optics. The aim of the current study is to investigate the changes in peripheral refraction and aberration in children wearing orthokeratology (study group) and single-vision spectacles (control group).

Enrollment: 90 patients

Sex: All

Ages: 6 to 9 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Myopia (refractive sphere): > 0.50D and ≤ 6.00D
• Astigmatism: with-the-rule astigmatism (axes 180 +/- 30) ≤ 1.50D; astigmatism of other axes ≤ 0.50D
• Spherical equivalent (SE): > 0.50D and ≤ 6.75D (myopia)
• Best corrected monocular visual acuity: equal to or better than 6/7.5 in Snellen scale
• Willingness to wear contact lenses or spectacles on a daily basis
• Availability for follow-up for at least 2 years

Exclusion criteria

• Strabismus at distance or near
• Contraindication for contact lens wear and orthokeratology (e.g. limbus to limbus corneal cylinder and dislocated corneal apex)
• Prior experience with the use of rigid lenses (including orthokeratology)
• Prior experience with myopic control treatment (e.g. refractive therapy or progressive spectacles)
• Systemic or ocular conditions which may affect contact lens wear (e.g. allergy and medication)
• Systemic or ocular conditions which may affect refractive development (e.g. Down syndrome, ptosis)

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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90 participants in 2 patient groups

Orthokeratology

Experimental group

Description:

Myopic children wearing orthokeratology at night will be the study group

Treatment:

Device: Orthokeratology lenses

Others

Other group

Description:

Myopic children wearing single-vision spectacles in the daytime will serve as control group

Treatment:

Device: Spectacles