Actively Recruiting
Objective Grading of Intraocular Inflammation in Uveitis Using Optical Coherence Tomography
Led by Oregon Health and Science University · Updated on 2025-07-17
125
Participants Needed
1
Research Sites
13 weeks
Total Duration
On this page
Sponsors
O
Oregon Health and Science University
Lead Sponsor
N
National Eye Institute (NEI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating a new method using a high resolution imaging device called optical coherence tomography (OCT) to count and classify different types of cells and proteins involved in anterior uveitis, which is inflammation in the front part of the eye caused by various systemic diseases. The study aims to create an unbiased, standard way to measure and understand this eye condition. This observational study includes participants with different eye conditions and healthy controls to compare findings. Participants are divided into three groups: those with active inflammation from diseases like spondyloarthritis, juvenile idiopathic arthritis, herpes simplex virus uveitis, birdshot chorioretinitis, Behcet disease, sarcoidosis, or other types of uveitis; those with vitreous floaters and posterior vitreous detachment; and healthy individuals with no history of eye inflammation, vitreous detachment, or eye surgery. The study uses OCT imaging to assess these groups and gather detailed eye cell and protein data. During the study, participants undergo OCT imaging and related eye assessments on Day 1 to identify and measure anterior chamber cells, flare, keratic precipitates, vitreous cells, and vitreous haze. The study tracks these eye inflammation markers without any treatment intervention. Participants must be between 5 and 85 years old and able to maintain steady eye fixation during imaging. The study continues until December 2026, with all visits and evaluations documented for research purposes.
CONDITIONS
Brief Title
Quantification & Classification of Inflammatory Cells in Uveitis Using OCT
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Eyes with active intraocular inflammation diagnosed with spondyloarthritis/HLA-B27 associated anterior uveitis, juvenile idiopathic arthritis associated chronic anterior uveitis, herpes simplex virus anterior uveitis, birdshot chorioretinitis, Behcet disease uveitis, sarcoidosis associated uveitis, other types of uveitis, or uveitis masquerade
- Eyes with vitreous floaters and posterior vitreous detachment
- Healthy eyes with no history of uveitis, posterior vitreous detachment, or previous eye surgery
- Participants aged between 5 and 85 years
You will not qualify if you...
- Unable to give informed consent
- Unable to maintain stable eye fixation for OCT imaging
- Unable to commit to all required study visits
- Pregnant or breastfeeding
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 optical coherence tomography imaging to assess and quantify inflammatory cells and related markers in the eye.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Casey Eye Institute - Oregon Health & Science University
Portland, Oregon, United States, 97239
Actively Recruiting
Research Team
H
Humberto Martinez, COT, MBA
D
Denzil Romfh, OD
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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