ClinicalTrials.gg
RecruitingNCT07065747Updated Jul 17, 2025

Quantification & Classification of Inflammatory Cells in Uveitis Using OCT

An observational study in Anterior Uveitis (AU), Birdshot Chorioretinitis and Behcet Disease, sponsored by Oregon Health and Science University. Recruiting at 1 site in United States. Open to participants aged 5 Years to 85 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-07-17.

Primary conditionBehcet SyndromeRegistry: Uveitis, AnteriorReclassifiedWhy we changed it
Registry
Uveitis, Anterior — the first condition term the registry derived for this study.
ClinicalTrials.gg
Behcet Syndrome
Why
  1. The study's listed conditions name Behcet Syndrome, a narrower term within Uveitis, Anterior.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Oregon Health and Science University · Observational

From the registry’s dates

  • Started Sep 2024; still recruiting 2 years 2 months later.
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
125
Ages
5 Years to 85 Years
Sex
All
01

Study summary

The goal of this study is to determine if it's possible to use a high resolution imaging device called optical coherence tomography (OCT) to develop an unbiased, standard method of counting and categorizing the various types of cells and proteins found in an eye condition called anterior uveitis. Anterior uveitis is a type of inflammation in the eye that can be caused by many different diseases of the body.

02

Conditions studied

  • Anterior Uveitis (AU)
  • Birdshot Chorioretinitis
  • Behcet Disease
  • Herpes Simplex Virus
  • Juvenile Idiopathic Arthritis (JIA)
  • Spondyloarthritis (SA)
  • Sarcoidosis
  • Posterior Vitreous Detachment
03

In context

Behcet Syndrome Reclassified

136 studies on the registry are indexed under Behcet Syndrome; 42 are open to participants now.

This study's planned enrollment of 125 is above the median of 90 across 63 observational studies indexed under Behcet Syndrome.

Browse Behcet Syndrome studies →

Lead sponsor

Oregon Health and Science University is the lead sponsor of 696 studies on the registry; 131 are open to participants now.

Of its 52 completed or terminated interventional studies of FDA-regulated products, 39 (75%) have results posted.

Compared within Behcet Syndrome, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Uveitis, Anterior. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
5 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Study participants will be recruited from clinical practices of the investigators at Casey Eye Institute of Oregon Health \& Science University in Portland, Oregon.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Uveitis Group: Eyes with active intraocular inflammation and a clinical diagnose of spondyloarthritis/HLA-B27 associated anterior uveitis, Juvenile Idiopathic Arthritis (JIA) associated chronic anterior uveitis, Herpes Simplex Virus (HSV) anterior uveitis, Birdshot chorioretinitis, Behcet disease uveitis, sarcoidosis associated uveitis, uveitis of any additional type, or uveitis masquerade.
  2. Posterior Vitreous Detachment Group: Eyes with vitreous floaters and posterior vitreous detachment (PVD).
  3. Healthy/Control Group: Healthy eyes with no history of uveitis, PVD, or previous eye surgery.

Exclusion criteria

Exclusion Criteria:

  1. Inability to give .
  2. Inability to maintain stable fixation for OCT imaging.
  3. Inability to commit to required visits to complete the study.
  4. Pregnancy and breastfeeding.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
125 participants (estimated)
Patient registry
No

Groups and cohorts

  • Uveitis Group

    Eyes with active inflammation due to various systemic diseases

  • Posterior Vitreous Detachment Group

    Eyes with vitreous floaters and posterior vitreous detachment

  • Healthy/Control Group

    Healthy eyes with no history of uveitis, posterior vitreous detachment, or previous eye surgery

06

What researchers measure

Primary outcomes

  1. Identification & Measurement of Anterior Chamber Cells

    Anterior Chamber (AC) cells will be identified from OCT images by computer algorithms. AC cell number counted by OCT will be correlated with slit lamp grading. Cell size \& other characteristics identified from OCT images will be associated with different uveitis diagnostic categories. The Standardization of Uveitis Nomenclature (SUN) grading system (scale: 0 = none to 4+ = severe) will be used to compare OCT-derived quantification against slit-lamp grading performed by attending physicians.

    Time frame: Day 1

Secondary outcomes

  1. Measure of AC Flare

    OCT signal of the aqueous humor will be analyzed and correlated with slit lamp grading by the attending physician. The SUN grading system (scale: 0 to 4+) will be used.

    Time frame: Day 1

  2. Measure of Keratic Precipitates

    Keratic precipitates (KPs) will be identified from OCT images. The size of the KPs will be compared across different uveitis diagnostic categories. There is no formal grading system for KPs. The investigators will use the typical qualitative assessments of morphology, distribution, and density. For morphology, cells will be described as fine, mutton-fat, stellate, or pigmented. Distribution patterns will be described as Arlt's Triangle, diffuse, central, or ring-shaped. Density will be described as few, moderate, or numerous.

    Time frame: Day 1

  3. Measure of Vitreous Cells

    Vitreous cells will be identified from OCT images. Counting of vitreous cells will be done by computer algorithms. Since vitreous cells are not formally graded or quantified in the SUN system, physician grading will be described as rare, few, moderate, numerous, or sheets and compared against the OCT-derived measurements.

    Time frame: Day 1

  4. Measurement of Vitreous Haze

    OCT signal of the vitreous clarity will be compared against clinical grading of vitreous haze. The National Eye Institute (NEI) Grading Scale will be used. Grading will be documented on a scale of 0 = no haze to 4+ = severe haze.

    Time frame: Day 1

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Sep 2024 (actual). Primary completion is estimated for Sep 2026, 24 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 2, 2025
First posted
Jul 15, 2025
StartActual
Sep 1, 2024
Primary completionEst.
Sep 2026
CompletionEst.
Dec 2026
Last update
Jul 17, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 17, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07065747
Responsible party
David Huang (Professor, Oregon Health and Science University) — Principal investigator
First posted
Jul 15, 2025
Start date
Sep 1, 2024
Primary completion
Sep 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Jul 17, 2025

Study contacts

Humberto Martinez, COT, MBA
Contact
martinhu@ohsu.edu
503-494-7712
Denzil Romfh, OD
Contact
romfhd@ohsu.edu
503-494-4351
Yan Li, PhD
principal investigator · Oregon Health and Science University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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