Ocular Blood Flow Imaging for Glaucoma Assessment
University of Maryland, Baltimore · with National Eye Institute (NEI), Vasoptic Medical, Inc · NCT05726058
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–88 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 150
- US sites recruiting
- 1
- Study start
- March 30, 2023
- Record last updated
- July 2, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The goal of this clinical trial is to investigate the use of an FDA-cleared retinal blood flow imaging instrument called the XyCAM RI and XyCAM FC (Vasoptic Medical, Inc., Columbia, MD) in glaucoma management.
The main question it aims to answer are
- Can the investigators use blood flow to discriminate between eyes with early-stage glaucoma and variable-matched controls?
- Can the investigators validate that the XyCAM FC simultaneously captures both stereo fundus photography and ocular blood flow monitoring?
Participants will be
- measured for their blood pressure, heart rate, height, and weight
- dilated with tropicamide
- imaged using the XyCAM RI, fundus photography, optical coherence tomography, and standard automated perimetry
- imaged using the XyCAM RI while inhaling 100% oxygen through a mask
Being studied: XyCAM with oxygen
Conditions: Glaucoma
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Age 18 and older with binocular vision
- Able to provide informed consent
- Patient is a healthy control OR is recommended for glaucoma assessment OR diagnosed with moderate to severe glaucoma in at least one eye as determined by Hodapp Anderson Criteria
Exclusion Criteria
- The subject has significant media opacity (e.g., a visually significant cataract or significant corneal scar)
- The subject has previous ocular surgery other than uncomplicated cataract extraction, laser trabeculoplasty (ALT or SLT), or YAG capsulotomy
- The subject has prior ocular disease other than glaucoma
- The subject has anatomically narrow angles or a prior adverse reaction to administration of Tropicamide or fluorescein dye
- The subject has more than 15 diopters of refractive error
- The subject is a female who is pregnant or nursing
- The subject has diabetes mellitus
Recruiting US locations
University of Maryland Eye Associates at Redwood
Baltimore, MD 21201
Site contact: Osamah Saeedi, MD, MS
Study contacts (from the official record)
- Osamah J Saeedi, MD, MS · (410) 328-5929 · osaeedi@som.umaryland.edu
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