H53.0
Conditions
Interventions
Group 1: Based on 198 study participants, we chose a post-hoc design for therapy control, in which a sample of 55 patients was selected according to the criterion of strong therapy resistance to occlu
Sponsors
Universitätsklinikum Carl Gustav Carus
Eligibility
Sex/Gender
All
Age
4 Years to 12 Years
Inclusion criteria
Inclusion criteria: Amblyopic patients (visual difference in the eyes > 0.1 logMAR or visual acuity <0.1 logMAR in the lazy eye) with anisometropia, anisometropia in connection with a strabism, or amblyopic patients with a strabism are included in the study. It is required that these patients are at least 4 years old.
Exclusion criteria
Exclusion criteria: No patients with other ophthalmological pre-existing diseases and no patients with deprivation amblyopia (amblyopia of organic cause) can be included in the study. Patients with proven learning disabilities must also be excluded. Patients with known epilepsy must also be excluded from Caterna visual training.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Effectiveness of amblyopia treatment with occlusion + FAVAS [ Time Frame: 6 months ] in amblyopic eyes in far vision single optical characters compared to occlusion alone | — |
Secondary
| Measure | Time frame |
|---|---|
| 2. Effectiveness of amblyopia treatment with occlusion + FAVAS [ Time Frame: 6 months ] amblyopic eyes increase in near vision by rows of optical characters compared to occlusion alone 3. Pre-/post differences in logarithmic steps (dB) of the far visual acuity assessed by single optical characters for the preceding occlusion alone normalized by recalculation in relation to a span of 6 months versus for the computer training combined with occlusion | — |
Countries
Germany
Contacts
Public ContactLydia Schurig
Universitätsklinikum Carl Gustav Carus
Outcome results
None listed