Discontinuation of Orthokeratology on Eyeball Elongation in Myopic Children (DOEE1)
Myopia
About this trial
This is an interventional treatment trial for Myopia focused on measuring children, corneal reshaping, myopia, myopia progression, orthokeratology
Eligibility Criteria
Inclusion Criteria:
- Age 8-14 years old (inclusive)
- Subjects who have completed the ROMIO, TO-SEE or HM-PRO studies at The Hong Kong Polytechnic University
- Willingness to be randomized into groups (for ortho-k subjects)
- Availability for follow-up for at least 14 months
Exclusion Criteria:
- Non-compliance to the follow up schedule
- Non-compliance to the assigned optical correction (i.e. single-vision glasses or ortho-k lenses)
- Contraindication for contact lens wear and ortho-k (e.g. limbus to limbus corneal cylinder and dislocated corneal apex)
- 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)
Sites / Locations
- School of Optometry, The Hong Kong Polytechnic University
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
Other
single-vision glasses and ortho-k lenses
ortho-k lenses
single-vision glasses
Children who are currently wearing ortho-k lenses at night for correction of refractive errors will be switched to wear single-vision glasses for the first 7 months and then switched back to ortho-k lenses for the next 7 months
Children who are currently wearing ortho-k lenses at night for the correction of refractive errors will continue with the current treatment and serve as the first control group
Children who are currently wearing single-vision spectacles in the daytime for correcting their refractive errors will continue with the current treatment and serve as the second control group