Sensitivity and specificity of an AI-based glaucoma screening

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00033058

Enrollment

150

Registered

2023-11-16

Start date

2023-11-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

H40

Interventions

Group 1: Glaucoma patients: 1 fundus and 1 optic disc photo, comparison of results (positive or negative) from software and ophthalmologist Group 2: healthy subjects: 2 fundus and 2 optic disc photo,

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Glaucoma patients (diagnosed using OCT, perimetry, clinical examination, pachymetry, intraocular pressure measurement)

Exclusion criteria

Exclusion criteria: No consent

Design outcomes

Primary

Measure	Time frame
Sensitivity: how many patients who are actually affected are reliably recognized as ill (positive test result), comparison of software result with evaluation by ophthalmologist, resident doctor and student, evaluation after data collection	—

Secondary

Measure	Time frame
Specificity: how many healthy subjects are reliably identified as healthy (negative test result), comparison of software result with evaluation by ophthalmologist, resident doctor and student, evaluation after data collection	—

Countries

Germany

Contacts

Public ContactAndreas Frings

Heinrich-Heine-Universität Düsseldorf

andreas.frings@med.uni-duesseldorf.de+49 911 235 558 25

Outcome results

None listed

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