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Binocularity stimulating treatment in patients with amblyopia

Binocularity stimulating treatment in patients with amblyopia

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0005150
Enrollment
38
Registered
2020-06-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Behavioral : In the test group, binocular treatment is performed at both eyes, and the control group is treated with occlusion. The biggest difference between the two groups is the difference between

Sponsors

Jeonbuk National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: i. Subjects with residual amblyopia defined as no more vision improvement following patching for at least 6 months at Chonbuk National University Hospital in South Korea. ii. When both the study subject and the representative of the study have received sufficient explanation (test process, possible side effects, etc.) to understand this and voluntarily agree to participate in the study.

Exclusion criteria

Exclusion criteria: A. Subjects diagnosed with systemic diseases such as congenital brain disease B. Subjects too young to test or understand the contents C. Subjects with other ophthalmic diseases (cataract, glaucoma, congenital optic nerve disease, etc.) that may affect vision or binocular function D. Subjects with a history of eye trauma E. Subjects with chronic neurological symptoms, such as headache and dizziness F. In addition to the above, if it is determined that the clinical research is difficult due to the judgment of the person in charge of the clinical research

Design outcomes

Primary

MeasureTime frame
Visual acuity

Secondary

MeasureTime frame
Stereopsis

Countries

Korea, Republic of

Contacts

Public ContactHAENGJIN LEE

Jeonbuk National University Hospital

leehaengjin@hanmail.net+82-63-250-1399

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026