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Artificial Intelligence for Staging Glaucoma Severity: A Comparison With an Eye Specialist Using Visual Field Tests

Reliability of Artificial Intelligence in Glaucoma Severity Staging Using the Brusini GSS2 System: A Longitudinal Comparative Study Against Expert Assessment

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07820709
Acronym
AI-GSS2
Enrollment
50
Registered
2026-09-15
Start date
2011-04-15
Completion date
2025-07-24
Last updated
2026-09-15

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

Conditions

Glaucoma and Ocular Hypertension

Brief summary

The study titled "Reliability of Artificial Intelligence in Glaucoma Severity Staging Using the Brusini GSS2 System: A Longitudinal Comparative Study against Expert Assessment" aims to evaluate the diagnostic reliability and clinical utility of an Artificial Intelligence (AI) system in staging glaucoma severity using the Brusini Glaucoma Staging System 2 (GSS2) compared to expert ophthalmologist assessment. The study protocol involves the longitudinal analysis of visual fields (VFs) collected at baseline (T0) and at a 1-year follow-up (T1). Statistical methodology will utilize quadratic weighted Cohen's kappa to assess diagnostic agreement between the AI system and expert assessment, Wilcoxon signed-rank tests to evaluate potential systematic bias, and Spearman's rank correlation to investigate the relationship between longitudinal progression and changes in the clinical Visual Field Index.

Interventions

DIAGNOSTIC_TESTArtificial Intelligence GSS2 Staging

An artificial intelligence system used to automatically stage glaucoma severity from standard automated visual field tests according to the Brusini Glaucoma Staging System 2 (GSS2). AI classifications were compared with those of an expert ophthalmologist at baseline and 1-year follow-up. The AI was used for assessment only and did not influence patient management or treatment.

Sponsors

University of Salerno
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL

Inclusion criteria

* Adults (≥18 years of age). * Diagnosis of glaucoma or suspected glaucoma undergoing routine clinical follow-up. * Availability of reliable standard automated visual field (VF) examinations at baseline and approximately 1-year follow-up. * Visual field tests suitable for staging using the Brusini Glaucoma Staging System 2 (GSS2). * Availability of all clinical data required for study analysis.

Exclusion criteria

* Unreliable visual field examinations (e.g., excessive fixation losses, false-positive or false-negative responses according to institutional reliability criteria). * Visual field defects attributable to ocular or neurological diseases other than glaucoma. * Missing baseline or follow-up visual field examinations. * Incomplete clinical data preventing GSS2 staging or statistical analysis. * Previous ocular conditions or interventions that could significantly affect visual field interpretation, if judged by the investigator.

Design outcomes

Primary

MeasureTime frameDescription
Quadratic weighted Cohen's kappa coefficient for diagnostic agreement in glaucoma severity staging between AI and expert assessmentBaseline (T0) and 1-year follow-up (T1)Glaucoma severity will be staged (from Stage 0 to Stage 5) using the Brusini Glaucoma Staging System 2 (GSS2) based on visual field parameters. Staging will be performed independently by the AI system and an expert ophthalmologist at each time point. Inter-rater agreement between the AI and expert staging will be quantified using the quadratic weighted Cohen's kappa ($\\kappa$), where values range from -1 (complete disagreement) to +1 (perfect agreement).

Secondary

MeasureTime frameDescription
Median difference in Brusini GSS2 staging scores between AI and expert assessmentBaseline (T0) and 1-year follow-up (T1)Differences in Brusini Glaucoma Staging System 2 (GSS2) staging scores (ranging from Stage 0 to Stage 5) assigned by the AI system versus the expert ophthalmologist will be evaluated to detect systematic overestimation or underestimation of disease severity. Paired score differences (AI minus Expert) at each time point will be reported and statistically tested using the Wilcoxon signed-rank test.

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 16, 2026