Actively Recruiting

Age: 18Years +
All Genders
ID06274593

Study of OCT Peripapillary Angiography to Monitor Progression in Patients with Advanced Glaucoma

Led by Nantes University Hospital · Updated on 2025-01-16

50

Participants Needed

2

Research Sites

174 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Glaucoma is a chronic eye disease that causes progressive damage to the optic nerve and loss of vision, making it the second leading cause of blindness worldwide and the leading cause of irreversible blindness. This research investigates how advanced glaucoma progresses over three years by comparing three different tests: a functional test called the visual field exam and two anatomical imaging methods called OCT angiography (OCTa) and OCT retinal nerve fiber layer thickness (OCTrnfl). These tests help to understand changes in nerve and blood vessel health in the eye. Participants will undergo peripapillary angiography using OCT at the start of the study and then annually for three years. This non-invasive imaging technique measures the density of blood vessels around the optic nerve head. Alongside this, the visual field test and OCTrnfl measurements will be used to monitor changes in vision and nerve fiber thickness. The study aims to assess how these measurements change over time in patients with advanced glaucoma. During the study, participants will be regularly evaluated using these imaging and functional tests to track disease progression. Researchers will measure changes in vascular density, optic nerve fiber thickness, and visual field loss over three years. The findings will help determine which tests best detect progression in advanced glaucoma. Safety and quality of imaging will also be monitored, with total participation lasting three years.

CONDITIONS

Official Title

Study of OCT Peripapillary Angiography in Patients With Advanced Glaucoma

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Men and women aged 18 and over
  • Patient with glaucoma followed in the ophthalmology department of Nantes University Hospital
  • Mean visual field deficit (MD) greater than 10 dB
Not Eligible

You will not qualify if you...

  • Retinal vascular pathologies such as moderate to severe non-proliferative diabetic retinopathy, complicated diabetic retinopathy, retinal vein or artery occlusions
  • Non-glaucomatous optic neuropathy or neurological conditions causing visual field deficits
  • Retinal panphotocoagulation or retinal cerclage
  • Retinal diseases causing visual field impairment like retinitis pigmentosa
  • Age-related macular degeneration and other macular diseases causing central vision loss
  • Significant eye conditions impairing imaging such as active uveitis or dense cataract
  • Loss of fixation point preventing visual field testing
  • Pregnant or breastfeeding women
  • Adults under guardianship or curatorship
  • Unreliable visual fields with false positives or negatives over 33%
  • Uninterpretable OCT retinal nerve fiber layer or OCT angiography due to artifacts or low quality

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 2 locations

1

CHU Nantes

Nantes, France, 44000

Actively Recruiting

2

Jean-Baptiste Ducloyer

Nantes, France, 44093

Not Yet Recruiting

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Research Team

J

Jean-Baptiste Ducloyer, M.D

I

Isabelle Orignac, M.D

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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