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Study identifier: NCT06353542 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Barcelona Esquerra Glaucoma Artificial Intelligence-based Screening Program (BEGAS)

Condition: Glaucoma  ·  Sponsor: Hospital Clinic of Barcelona

PhaseNA
Planned participants500
Who can joinAll sexes, 40 Years to 80 Years
Healthy volunteersYes

About this study

Two primary care-based screening systems will be tested to identify subjects with referrable glaucoma to hospital care. Subjects between 45 to 64 years old living in the metropolitan area of Barcelona will be invited to participate in a one-time visit, with an optic disc examination and intraocular pressure (IOP). The criteria for referring a patient will be the detection of glaucoma but with two different approaches depending on which Integrated Practice Unit (IPU) the patients will be allocated to: one arm using an Artificial Intelligence (AI) reading software of the optic disc picture; and the other one will base their referral after an ophthalmic examination performed by an ophthalmologist. In both circuits, an optic nerve head photography will be obtained, and a masked reading center will be established to determine the ground truth for diagnosis. This screening trial will explore the level of agreement between both systems and the cost-effectiveness of each of them. Secondary analyses will include potential diagnostic composite scores (including other ancillary tests, such as optical coherence tomography images, that could maximize the screening process); the identification of population and disease characteristics (type of glaucoma, intraocular pressure) that could increase the effectivity and adherence to the screening process.

This description comes directly from the study's public registry record.

Talk to the study team

Nestor Ventura Abreu, MD, PhD  ·  +34932275400  ·  neventura@clinic.cat

Always discuss trial participation with your own doctor first.

Locations (1)

Hospital Clínic - ICOFBarcelona, Barcelona, SpainRecruiting

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Source record: clinicaltrials.gov/study/NCT06353542