Actively Recruiting
Assessment of Endothelial Glycocalyx in Patients With Primary Open-angle Glaucoma: a Prospective Single-center Cross-sectional Case-control Study
Led by Fondation Ophtalmologique Adolphe de Rothschild · Updated on 2025-12-08
100
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are exploring the role of the endothelial glycocalyx, a protective lining inside blood vessels, in patients with primary open-angle glaucoma, a chronic eye disease that damages the optic nerve and affects vision. The study focuses on the ischemic theory of glaucoma, which suggests that reduced blood flow to the optic nerve contributes to disease progression. The glycocalyx has been linked to vascular health in various conditions but is less studied in glaucoma. The study uses a special imaging technique called GlycoCheck to assess the microvascular system's health by measuring a MicroVascular Health score (MVHS). This score includes parameters such as capillary density, red blood cell filling percentage, and the thickness of the perfused boundary region (PBR). Participants are divided into two groups: those with primary open-angle glaucoma and those without any optic nerve pathology. Ophthalmological exams including visual acuity, eye pressure, corneal thickness, retina imaging, and visual field tests are also conducted. Participants will undergo these non-invasive assessments, including GlycoCheck and detailed eye exams, to evaluate blood vessel health and optic nerve status. Researchers will measure the thickness of the perfused boundary region as the primary outcome to better understand vascular changes in glaucoma. The study aims to provide insights into the microvascular system's role in this eye condition. Participation involves a one-time observational visit, with no treatment administered, and study-related procedures are designed to be safe and painless.
CONDITIONS
Brief Title
Assessment of Endothelial Glycocalyx in Patients With Primary Open-angle Glaucoma
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Express consent to participate in the study
- For case group: primary open angle glaucoma with visual field damage in both eyes
- For control group: no optic nerve pathology including glaucoma
- Adults aged 18 years or older
You will not qualify if you...
- Pregnant or breastfeeding women
- Sleep apnea
- Renal insufficiency
- Parkinson's disease
- Alzheimer's disease
- Antiphospholipid syndrome
- Cancer treated less than 2 years ago
- Stroke less than 1 year ago
- Myocardial infarction less than 1 year ago
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo assessments including sublingual microvascular imaging and ophthalmological examinations to evaluate microvascular system integrity and eye health.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Hôpital Fondation A. de Rothschild
Paris, France, 75019
Actively Recruiting
Research Team
A
Amélie YAVCHITZ, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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