Uveitis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You have active eye inflammation and have been diagnosed with one of several specific eye conditions linked to conditions such as spondyloarthritis, juvenile idiopathic arthritis, herpes simplex virus, or other types of uveitis (an inflammation inside the eye).
- You have floaters in your vision caused by a condition where the gel inside your eye has pulled away from the back of the eye (called posterior vitreous detachment).
- You have healthy eyes with no history of eye inflammation, the gel pulling away from the back of your eye, or any previous eye surgery (for a healthy volunteer/control group).
Who may not be able to join:
- You are not able to give your agreement to take part in the study after being informed about it.
- You are not able to keep your eye still enough during the eye scanning procedure used in this study.
- You are not able to commit to attending all the required visits for the study.
- You are currently pregnant or breastfeeding.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Yan Li, PhD, Oregon Health and Science University
Phone: 503-494-7712
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Identification & Measurement of Anterior Chamber Cells
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.