Enhancement of Emmetropization in Highly Hyperopic Infants
Hyperopia
About this trial
This is an interventional treatment trial for Hyperopia focused on measuring Emmetropization, Refractive Error, Glasses, Accommodation
Eligibility Criteria
Inclusion Criteria:
- Age: between 8 and 15 weeks at baseline examination
- Either gender
- Any ethnicity
- Birthweight greater than 2500g
- Normal pregnancy and delivery (including Cesarean section delivery but excluding serious complications or conditions such as eclampsia or rubella)
- Hyperopia greater than or equal to +5.00 Diopters (D) in the spherical component of refractive error in one or both eyes measured with cycloplegic retinoscopy using 1% cyclopentolate
- Infants with a refractive error of greater than or equal to +5.00D but less than or equal to +7.00D in the spherical component of refractive error will be randomized to treatment (partial correction with accommodative training) or observation only.
- Infants with greater than +7.00D in the spherical component of refractive error will receive treatment
Exclusion Criteria:
- Astigmatism greater than 2.00D in either eye
- Anisometropia greater than 1.50D (spherical equivalent)
- History of strabismus surgery
- History of difficulty with pupillary dilation
- History of cardiac, liver, asthma, or other respiratory disease
- History of ocular disease, retinal detachment, severe macular dragging, intraocular surgery, optic nerve hypoplasia, malformations of the eye, cortical visual impairment or active inflammation
- History of hydrocephalus, Down syndrome, cerebral palsy, developmental delay, seizure disorders
Sites / Locations
- The Ohio State University
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
No Intervention
Active Comparator
Hyperopic subjects receiving glasses
Hyperopic subjects uncorrected
Highly hyperopic subjects corrected
Randomized +5.00 to +7.00 diopter hyperopic subjects that will receive partial refractive correction and will be instructed to do accommodation exercises on a daily basis.
Randomized +5.00 to +7.00 diopter hyperopic subjects that will serve as the control to the experimental arm who will receive no correction but be observed for the duration of the study.
If a subject is found to be greater than +7.00 diopters hyperopic during the screening phase of the study, they will receive glasses correction and be followed during the study period.