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Taking people in FranceNo phase

Brain scans over time in people with glaucoma and healthy volunteers

Uses brain MRI scans to compare brain changes in glaucoma patients and controls.

Plain-language title generated from the registry record
Registry title: Magnetic Resonance Imaging of Cerebral Connectivity and Volume in Neurodegeneration and Glaucoma

Key facts

Where
Bordeaux, FranceSee the site

Where in France

  • CHU BordeauxBordeaux, FranceTaking people

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Trial details

Who runs it
University Hospital, Bordeaux
Trial code
NCT07802769
Record updated
3 September 2026
Original description
The EVOLUTION is a 10-year extension of the ENVOL study. It seeks to compare the evolution of structural and functional connectivity (Hub Disruption Index) and cerebral volume on 3T MRI of the brain in glaucoma patients and matched controls. The study aims to examine the hypothesis that glaucomatous optic neuropathy is not limited solely to the visual pathway, but rather is associated with a broader degeneration of the central nervous system.Read full original descriptionShow less

Magnetic Resonance Imaging of Cerebral Connectivity and Volume in Neurodegeneration and Glaucoma

The EVOLUTION is a 10-year extension of the ENVOL study. It seeks to compare the evolution of structural and functional connectivity (Hub Disruption Index) and cerebral volume on 3T MRI of the brain in glaucoma patients and matched controls. The study aims to examine the hypothesis that glaucomatous optic neuropathy is not limited solely to the visual pathway, but rather is associated with a broader degeneration of the central nervous system.

Inclusion: having been previously included and completed the ENVOL study; Ability and willingness to provide informed consent; Having a valid health insurance in France; In glaucoma group :; Glaucomatous optic neuropathy, being able to be graded by the vertical C/D ratio; Open angle on gonioscopy in a dark-room testing according to Shaffer's classification (grade 3 or grade 4); Visual field impairement (at least one of the following) :; 3 adjacent points with at least 5dB loss; one point with a loss of 10dB; a difference of at least 10 dB for 2 adjacent points on either side of the horizontal meridian of the nasal visual field; Mini Mental State Score of at least 28; In control group :; No personal or family history of glaucoma or ocular hypertension (IOP > 21 mmHg); Open angle on gonioscopy in a dark-room testing according to Shaffer's classification (grade 3 or grade 4); Intraocular pressure of ≤ 21 mmHg; Absence of glaucomatous neuropathy; Normal visual field.

Exclusion: Contraindications to MRI testing (pacemakers or neurosensory stimulators, cochlear implants, ferromagnetic foreign bodies, claustrophobia); Other causes of ocular hypertension (trauma, uveitis); Inability/unwillingness to provide informed consent; Non-glaucomatous optic neuropathy (infectious, inflammatory, compressive, ischemic); Unreliable visual field (>15% false positives, >33% false negatives or >20% loss of fixation); Severe corneal pathology preventing access to fundus, visual field testing or altering ocular tonometry; Patients under guardianship or other form of legal protection.

ClinicalTrials.gov NCT07802769