Evaluation of Progression of Myopia in Children Treated With Vitamin B2 and Outdoor Sunlight Exposure
Axial Myopia, Refractive Errors
About this trial
This is an interventional treatment trial for Axial Myopia focused on measuring Myopia, Axial Myopia, Children, Refractive Error, Riboflavin, Vitamin B2
Eligibility Criteria
Inclusion Criteria:
- Healthy children ages 6-12 years old with myopia more than 0.50 D and astigmatism no more than 1.5 D.
- Caretakers who choose to enroll their child in the study must agree to participate in the study on their own will after knowledge of potential alternatives (spectacle correction, orthokeratology, atropine eye drops, etc.) are explained to the patient's caretaker.
Exclusion Criteria:
- Known allergy to riboflavin
- Birth history of premature birth
- Developmental delay or other neurological or mental conditions
- Major systemic health problems
- Significant anisometropia more than 1.5 Diopters
- Any other eye condition which may complicate interpretation of data including: congenital glaucoma, congenital cataract, ectatic corneal condition, amblyopia or strabismus.
Sites / Locations
- Eye Institute EastRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Placebo Comparator
200 mg Riboflavin (oral)
400 mg Riboflavin (oral)
0 mg Riboflavin (oral)
These patients (approximately 1/3rd of all patients enrolled in the study) will be given 200 mg oral riboflavin each day for 6 months and be encouraged to play outside for 30 minutes a day every day.
These patients (approximately 1/3rd of all patients enrolled in the study) will be given 400 mg oral riboflavin each day for 6 months and be encouraged to play outside for 30 minutes a day every day.
These patients (approximately 1/3rd of all patients enrolled in the study) will be given 0 mg oral riboflavin (placebo) each day for 6 months and be encouraged to play outside for 30 minutes a day every day.