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GLAUcoma Diagnostic and Imaging Analysis (GLAUDIA) Study

I

Institute of Hospitalization and Scientific Care (IRCCS)

Status

Not yet enrolling

Conditions

Glaucoma Open-Angle Primary
Ocular Hypertension

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

This observational study aims to identify early diagnostic markers of glaucomatous damage by combining functional and structural assessments. Patients with primary open-angle glaucoma and ocular hypertension will undergo comprehensive ophthalmological evaluation, including visual field testing and multimodal imaging of the optic nerve and retina. Both retrospective and prospective data will be collected. The main objective is to define new diagnostic paradigms for detecting early glaucomatous changes and to improve the accuracy of current clinical practice in glaucoma management.

Enrollment

60 estimated patients

Sex

All

Ages

40 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age between 40 and 90 years.
  • Best-corrected visual acuity ≥ 0.1 LogMAR (≥ 8/10).
  • For primary open-angle glaucoma (POAG):
  • IOP ≥ 21 mmHg with normal visual field and/or normal optic nerve head/RNFL, or
  • Suspicious optic nerve head (excavation), or
  • Reproducible glaucomatous visual field defect.
  • POAG patients stratified by visual field mean deviation (MD): -3 to -10 dB (S1-S2 Brusini classification).

Exclusion criteria

  • Best-corrected visual acuity worse than 0.1 LogMAR (< 8/10).
  • Ocular surgery in the last 6 months (except uncomplicated cataract extraction).
  • Previous vitreoretinal surgery for macular pathologies (e.g., macular pucker, macular hole) or retinal detachment.
  • High myopia (> -3 diopters).
  • Optic disc anomalies not attributable to glaucoma (tilted disc, papillary drusen, other morphological/functional anomalies).
  • Severe motor disability preventing proper positioning for tests.
  • Cognitive impairment reducing test reliability.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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