Actively Recruiting
Study of Corneal Biomechanics in Glaucoma Patients Using Brillouin Microscopy
Led by University of Maryland, Baltimore · Updated on 2025-09-09
60
Participants Needed
1
Research Sites
39 weeks
Total Duration
On this page
Sponsors
U
University of Maryland, Baltimore
Lead Sponsor
N
National Eye Institute (NEI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This pilot study evaluates the biomechanical properties of the cornea in glaucoma patients using Brillouin microscopy, a non-contact imaging technique. The study aims to compare corneal stiffness between patients with normal-tension glaucoma, high-tension glaucoma, and healthy controls, and to assess changes in corneal biomechanics following intraocular pressure (IOP)-lowering treatment. The goal is to determine whether Brillouin-derived biomechanical measurements can serve as biomarkers for glaucoma risk and progression.
CONDITIONS
Official Title
Study of Corneal Biomechanics in Glaucoma Patients Using Brillouin Microscopy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Diagnosis of primary open angle glaucoma (POAG) or no history of glaucoma (for controls)
- Open angle on gonioscopy (Shaffer grade 3 or 4)
- Best-corrected visual acuity of 20/25 or better
- Refractive error between +3.00 and -5.00 diopters
- No prior use of topical glaucoma medications
- Diagnosis of High Tension Glaucoma (IOP 65 22 mmHg on 3 visits)
- Diagnosis of Normal Tension Glaucoma (IOP 64 21 mmHg on 3 visits)
- Age-matched control with normal optic nerve and visual fields
You will not qualify if you...
- Corneal abnormalities or conditions interfering with Brillouin or applanation tonometry
- Retinal diseases affecting RNFL (e.g., macular traction)
- History of ocular surgery or laser
- Diagnosis of diabetes
- History of uveitis
- History of prolonged steroid use
- Neurodegenerative or systemic diseases (e.g., multiple sclerosis, Alzheimer's, Parkinson's, schizophrenia)
- Unreliable visual fields
- Contraindications to beta blockers (e.g., bradycardia, severe pulmonary disease)
- Moderate to severe glaucoma (per Hodapp-Anderson-Parrish criteria)
- History of contact lens use
- Low blood pressure
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Maryland School of Medicine
Baltimore, Maryland, United States, 21201-1757
Actively Recruiting
Research Team
O
Osamah Saeedi, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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