CURESIGHT BINOCULAR AMBLYOPIA TREATMENT STUDY

Launched by NOVASIGHT · Mar 3, 2021

Keywords

ClinConnect Summary

Screening A child is considered for the study after undergoing a standard of care and study specific eye examinations (by a study investigator as part of standard of care) that identifies amblyopia appearing to meet the eligibility criteria. The study will be discussed with the child's parent(s) or guardian(s) (referred to subsequently as parent(s)). Parent(s) who express an interest in the study will be given a copy of the informed consent form to read. Written informed consent / assent must be obtained from a parent and child prior to performing any study-specific procedures that are not ...

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• The following criteria must be met for a child to be enrolled in the study:
• • 1. Age 4 to \<9 years male and female
• • 2. Amblyopia associated with strabismus, anisometropia, or both (previously treated or untreated)
• 1. Criteria for strabismic amblyopia: At least one of the following must be met:
• • Presence of a heterotropia on examination at distance or near fixation (with or without optical correction, must be no more than 5 PD by SPCT at near fixation
• • Documented history of strabismus which is no longer present (which in the judgment of the investigator could have caused amblyopia)
• 2. Criteria for anisometropia: At least one of the following criteria must be met:
• • ≥1.00 D difference between eyes in spherical equivalent
• • ≥1.50 D difference in astigmatism between corresponding meridians in the two eyes
• 3. Criteria for combined-mechanism amblyopia: Both of the following criteria must be met:
• • Criteria for strabismus are met (see above)
• • ≥1.00 D difference between eyes in spherical equivalent OR ≥1.50 D difference in astigmatism between corresponding meridians in the two eyes
• Amblyopia associated with anisometropia, strabismus or both meeting at least one of the following conditions:
• • Newly diagnosed amblyopia (i.e. no prior treatment)
• • Non-adherence to amblyopia treatment with no treatment administered for a minimum of 8 weeks prior to the Screening Visit
• 3. Must have refractive error correction (based on a cycloplegic refraction completed within the last 7 months) if any of the following are true:
• • Hypermetropia of 2.50 D or more by spherical equivalent (SE)
• • Myopia of amblyopic eye of 0.50D or more SE
• • Astigmatism of 1.00D or more
• • Anisometropia of more than 0.50D SE
• • NOTE: Subjects with cycloplegic refractive errors that do not fall within the requirements above for spectacle correction may be given spectacles at investigator's discretion, but must follow the study-specified prescribing guidelines, as detailed below.
• 1. Spectacle prescribing instructions referenced to the cycloplegic refraction completed within the last 7 months:
• • SE must be within 0.50D of fully correcting the anisometropia.
• • SE must not be under corrected by more than 1.50D SE, and reduction in plus sphere must be symmetric in the two eyes.
• • Cylinder power in both eyes must be within 0.50D of fully correcting the astigmatism.
• • Axis must be within +/- 10 degrees if cylinder power is ≤1.00D, and within +/- 5 degrees if cylinder power is \>1.00D.
• • Myopia must not be under corrected by more than 0.25D or over corrected by more than 0.50D SE, and any change must be symmetrical in the two eyes.
• 2. Spectacle correction meeting the above criteria must be worn:
• • For at least 16 weeks OR until distance VA stability is documented (defined as \<0.1 logMAR change by the same testing method measured on 2 consecutive exams at least 8 weeks apart).
• * For determining VA stability (non-improvement):
• • The first of two measurements may be made 1) in current spectacles, or 2) in trial frames with or without cycloplegia or 3) without correction (if new correction is prescribed),
• • The second measurement must be made without cycloplegia in the correct spectacles that have been worn for at least 8 weeks.
• • Note: since this determination is a pre-study procedure, the method of measuring VA is not mandated.
• 4. VA, measured in each eye without cycloplegia in current spectacle correction (if applicable) within 7 days prior to randomization using the Lea symbol per ATS VA protocol for children \< 7 years and the E-ETDRS VA protocol for children ≥ 7 years on a study-approved device displaying single surrounded optotypes, as follows:
• • 1. Visual acuity in the amblyopic eye 20/32 to 20/100 inclusive
• 2. Best-corrected dominant-eye VA meeting the following criteria:
• • If age 4, 20/40 or better by Lea symbol per ATS
• • If age 5 and older, 20/32 or better by ATS-HOTV using LEA symbols for age \<7 and Lea numbers for \> 7 years
• • 3. Interocular difference ≥ 2 logMAR lines (Lea symbol per ATS)
• • 5. Heterotropia with a near deviation of \<5∆ (measured by SPCT) in habitual correction (Angles of ocular deviation \>4∆ are not allowed because large magnitudes of the deviation would compromise successful alignment of the dichoptic stimuli.)
• • 6. Passing a dedicated 10 min in-clinic performance ability test to assure suitable eye tracking performance (validity of eye tracking data \>90% and successful calibration process).
• • 7. Subjects and families eligible for clinic visits over duration of study.
• • 8. Subject in general good health and able, as per investigator decision, to comply with study visits and protocol procedures and wear refractive correction and has access to wireless internet at home which is able to support the CureSight treatment (loaned by sponsor) .
• • 9. Signed and dated informed consent form.
• • 10. Parent and participant understand and are willing to comply with study procedures and will be available for the duration of the study.
• Exclusion Criteria:
• • 1. Myopia greater than -6.00 D. spherical equivalent in either eye.
• • 2. Known skin reactions to patch or bandage adhesives.
• • 3. Any other condition which could be a potential cause for reduced BCVA according to the investigator.
• • 4. Severe developmental delay that would interfere with treatment or evaluation (in the opinion of the investigator). Subjects with mild speech delay or reading and/or learning disabilities are not excluded.
• • 5. History of low adherence with amblyopia treatment as assessed informally by the investigator.
• • 6. Subjects that do not wear their spectacles. (as assessed by investigator)
• • 7. History of light-induced seizures.
• • 8. Wearing RGP contact lenses.
• • 9. Any reported anatomic ocular anomaly (e.g., small lens opacity, myelinated nerve fiber layer).
• • 10. Previous intraocular or refractive surgery.
• • 11. Any condition that prevents the subject from completing a continues 45-90 min. of treatment per day while seating in front of a near screen. Such as children who don't like or cannot watch TV/movies for more than 60 min every day according to the parent's report.
• • 12. Heterophoria with a total near deviation of ≥10Δ (measured by PACT).