Multi-center retrospective and prospective data analysis with additive app-based therapy to optimize amblyopia therapy

Recruiting

• Conditions: H53.0; Amblyopia ex anopsia

• Registration Number: DRKS00017633
• Lead Sponsor: Knappschaftsklinikum Saar GmbH

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-09-11
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

Amblyopic patients (visual acuity> 0.1 log MAR or visual acuity <0.1 log MAR in the poorer eye) are recorded with anisometropia, anisometropia associated with strabisme, or amblyopic patients with strabismus. It is required that these patients are at least 4 years old.

Through a Germany-wide network, we can also include retrospective data from Ophtalmologists who already have used the Caterna visual training in combination with occlusion therapy as an amblyopia therapy.

Exclusion Criteria

No patients with other pre-existing ophthalmologic conditions and patients with defensive amblyopia (weak-sightedness of organic cause) may be enrolled in the study. Patients with learning disabilities must also be excluded. Even patients with known epilepsy must be excluded from the Caterna Vision training.

Study & Design

• Study Type: observational
• Study Design: Not specified