Binocular Amblyopia Treatment

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

To evaluate the effectiveness of enhanced binocular amblyopia treatments in achieving a more complete and stable recovery.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 4
Maximum Age: 10
Healthy Volunteers: f
View:

• age 4-10 y

• male and female

• strabismic, anisometropic, or combined mechanism amblyopia

• amblyopic eye best-corrected visual acuity 0.3-0.8 logMAR

• fellow eye best-corrected visual acuity ≤0.1 logMAR

• interocular visual acuity difference ≥0.3 logMAR

• wearing glasses (if needed) for 8 weeks or no change visual acuity with glasses at 2 visits

⁃ 4 weeks apart.

• child's ophthalmologist and family must be willing to forgo patching treatment during the 12-week study period

• parent's informed consent

• child must demonstrate understanding and ability to play binocular games

Locations
United States
Texas
Retina Foundation of the Southwest
RECRUITING
Dallas
Contact Information
Primary
Reed Jost, MS
reedjost@retinafoundation.org
2143633911
Backup
Krista Kelly, PhD
kkelly@rfsw.org
2143633911
Time Frame
Start Date: 2017-08-31
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 120
Treatments
Active_comparator: Standard Contrast Increment
Experimental: Reduced Contrast Increment
Experimental: No Contrast Increment
Related Therapeutic Areas
Sponsors
Leads: Retina Foundation of the Southwest
Collaborators: National Eye Institute (NEI)

This content was sourced from clinicaltrials.gov

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