Evaluation of a tablet visual acuity test

Not Applicable

Recruiting

• Conditions: H53.0; Q13.1; Q13.3; E70.3; H35.1; H53.5; H50; Amblyopia ex anopsia; Absence of iris; Congenital corneal opacity

• Registration Number: DRKS00011508
• Lead Sponsor: niversitätsklinikum Essen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2016-12-20
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Age <6 years
Patient of our orthoptic department
Amblyopia, glaucoma, aniridia, cataract, strabism, albinism, achromatopsia, retinal dystrophies, atrophy of optic nerve

Exclusion Criteria

Age <2 years;
inadequate cooperation;
motor impairment which makes targeted movements impossible;
concomitant participation in pharmaceutical study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The agreement between the visual acuity measurements with established methods and the new tablet method will be evaluated.