Find Out If You Are Eligible

Understand Your Eyes Better with Advanced, Non-Invasive Imaging Tests

Gain insights of your eyes for future care

No impact on eye pressure

Compensation up to $140 provided for time & travel

Study conducted by Researchers from 

University of Maryland, Baltimore

Can a simple test today help prevent vision loss tomorrow? Glaucoma often progresses quietly, and small changes in the eye can go unnoticed until vision is affected. 


Researchers at the University of Maryland, Baltimore, are using a new, noninvasive imaging tool called the Brillouin microscope to study how the cornea’s stiffness changes in people with glaucoma. By understanding these subtle changes, this study could help doctors detect glaucoma earlier, guide better treatment decisions, and protect vision for the future.


Interested? Sign up today and make a difference for your eyes.

Why Participate?

Participant Tools and Equipment

  • Learn more about your eye health through advanced, noninvasive imaging tests at no cost.
  • Gain a better understanding of your eyes, which may be useful for your future care.

Compensation for Your Time

  • Receive $40 in gift cards for each completed visit, with additional compensation for optional follow-ups and travel support up to $100.

Support Critical Research

  • Contribute valuable information that could help researchers improve glaucoma management and support early detection.

Eligibility Requirements

Who Can Participate

  • Adults who are 18 years or older.
  • Must have been told by an eye doctor that they have an open angle (a normal drainage area in the eye).
  • Must have 20/25 vision or better, with or without glasses or contact lenses.
  • Must have a refractive error between +3.00 and −5.00 diopters (glasses or contact lens prescription between +3 and −5).

Who Cannot Participate

  • Those with corneal problems or other eye conditions that make pressure or imaging tests difficult.
  • Those with secondary glaucoma (glaucoma caused by another condition).
  • Those who have had eye surgery or laser treatment in the past.
  • Those who have used glaucoma eye drops before.
  • Those whose visual field test results have been unreliable, as determined by their eye doctor.
  • Those who have diabetes.
  • Those who have taken steroids for a long time that may have raised their eye pressure.
  • Those who have had uveitis (eye inflammation).
  • Those who have multiple sclerosis, Alzheimer’s disease, Parkinson’s disease, or schizophrenia.
  • Those who have serious lung problems or a slow heart rate that would prevent using certain glaucoma eye drops.
  • Those with low blood pressure (below 90/60 mm Hg).

Study Process

The study team will explain the research in its entirety, but some details include:

  • Participants will be asked to attend a one-time imaging visit, with the option to return for two additional imaging visits about 3 and 6 weeks after starting treatment, and a final imaging visit at approximately 3 months.
  • Participants will be asked to undergo Brillouin microscopy and, if they haven’t had a recent eye exam, complete standard eye tests such as tonometry, OCT, and visual field testing.
  • Participants will be asked to have their pupils dilated with Tropicamide eye drops if needed before testing, with all imaging expected to take about 40–70 minutes.

Meet the Lead Researcher

Osamah Saeedi, MD, MS

Osamah Saeedi, MD, MS, is an Associate Professor of Ophthalmology at the University of Maryland School of Medicine in Baltimore, MD, and an Adjunct Associate Professor of Bioengineering at the University of Maryland, College Park. Dr. Saeedi completed medical school and ophthalmology residency at the University of Texas – Southwestern Medical Center and glaucoma fellowship at the Wilmer Eye Institute, Johns Hopkins University. He completed a Master of Science in Epidemiology and Clinical Research. Dr. Saeedi is the recipient of an NIH Career Development Award (K23) and has grant funding from numerous other organizations, including the American Glaucoma Society. His research focuses on finding novel imaging biomarkers for glaucoma, specifically looking at new techniques for assessing ocular blood flow.

Study Location

This study involves in-person visits at

University of Maryland, Baltimore, Maryland, 21201, United States

At the University of Maryland, Baltimore, our core values demonstrate what we stand for and serve as a guide to how we behave. Our core values are Respect and Integrity, Well-Being and Sustainability, Equity and Justice, and Innovation and Discovery. The University of Maryland, Baltimore’s (UMB) core values are at the heart of our mission to improve the human condition and serve the public good of Maryland and society at large through education, research, clinical care, and service. These core values guide our academic programs, operating philosophy, and commitment to our constituents, while supporting our dedication to global enhancement and social progress.

Your Safety Comes First

IRB Approved

Ethics Approved Research Studies

This study has been reviewed and approved by the UMB IRB Office (HP-00110432)

Qualified Health Professionals

Qualified Study Professionals

Qualified health professionals will monitor your health as it relates to the study.

Trained Staff

Ethical Recruitment Practices

The Trialfacts team is GCP-trained, ensuring the rights, safety, and well-being of research subjects are protected.

HIPPA Compliant

Privacy Standards You Can Trust

We adhere to all national privacy standards used by doctors’ offices, hospitals, and medical institutions.

Your Safety Comes First

This study has been reviewed and approved by the Bellberry Human Research Ethics Committee (Project ID: GPNV-008)

Ethics Approved Research Studies

Qualified health professionals will monitor your health as it relates to the study.

Qualified Study Professionals

The Trialfacts team is GCP-trained, ensuring the rights, safety, and well-being of research subjects are protected.

Ethical Recruitment Practices

We adhere to all national privacy standards used by doctors’ offices, hospitals, and medical institutions.

Privacy Standards You Can Trust

Participant’s Rights

Informed Consent

You will receive a detailed outline of all details of the study, including risks and procedures, and you will be given the chance to ask study staff questions before you decide whether to participate.

Withdraw At Any Time

If you decide to participate in the study and later feel that you no longer wish to be part of it, you can withdraw at any time

Secure and Confidential Data

Your records relating to this study and any other information received will be kept strictly confidential, except as required by law.

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© 2025 Trialfacts. All Rights Reserved. | (415) 704-1575 USA | (07) 3054 7094 AUS support@trialfacts.com | Privacy Policy