Clinical Trial

Evaluation of BRUDYGLAUCO (DHA + Citicoline) in Patients With Glaucoma

Study acronym: BRUDYGLAUCO
Recruiting
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Summary
This study aims to evaluate the effects of BrudyGlauco, a nutritional supplement containing DHA (docosahexaenoic acid) and citicoline, on visual function in people with glaucoma. Glaucoma is a progressive optic neuropathy that can lead to vision loss. Current treatments focus on lowering eye pressure, but there are other pathogenic factors and the use of additional therapies that could protect or regenerate the optic nerve would be beneficial. This is a randomized, double-blind, placebo-controlled, and multicenter clinical trial. Participants will be randomly assigned to receive either BrudyGlauco or a placebo for 12 months. The study will assess changes in visual field, safety, and treatment adherence. The trial is being conducted at the Institut Català de Retina (ICR) and Hospital de la Esperanza. Participants will undergo regular eye exams, visual field tests, and follow-ups to monitor potential improvements in visual function. The results of this study will help determine if BrudyGlauco can provide neuroprotective benefits for people with glaucoma and improve their quality of life.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-12-23.
Trial Details
NCT Number NCT07322965
Lead Sponsor Institut Catala de Retina
Collaborators: Hospital de la Esperanza
Conditions Glaucoma, Primary Open Angle Glaucoma (POAG), Neuroprotection
Enrollment 108 participants
Start Date 2025-04-01
Primary Completion 2027-04-30 (estimated)
Study Completion 2027-05-30 (estimated)
Updated on ClinicalTrials.gov 2026-01-14