A Study of Uveitis in Children <18 Years of Age
UV1
1 other identifier
observational
300
1 country
4
Brief Summary
The goal of this observational study is to collect data regarding clinical features and current/past treatments in children under 18 with uveitis. The main questions it aims to answer are:
- What are the frequency of uveitis subtypes in children?
- What are clinical and demographic characteristics overall and within each type of uveitis? Participants will complete one enrollment visit with their doctor. Participants with uveitis onset \<6 months from enrollment date will also partake in a 12 month chart review.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2026
4 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 1, 2026
CompletedFirst Posted
Study publicly available on registry
April 8, 2026
CompletedStudy Start
First participant enrolled
April 14, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
April 1, 2028
May 8, 2026
May 1, 2026
12 months
April 1, 2026
May 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Frequency of uveitis subtypes in children <18 years of age
Enrollment
Study Arms (2)
Children diagnosed with uveitis - established cases
Children diagnosed with uveitis (onset \> 6 months), either active or inactive with or without current treatment at time of enrollment.
Children diagnosed with uveitis - incident cases
Children diagnosed with uveitis (onset ≤ 6 months), either active or inactive with or without current treatment at time of enrollment.
Eligibility Criteria
Children \<18 years with active or inactive uveitis.
You may qualify if:
- Age:
- Incident cases (onset ≤ 6 months) \<17 years
- Established cases (onset \> 6 months) \<18 years
- Diagnosis of any type of uveitis (infectious or noninfectious) in any location except traumatic and post-operative uveitis.
- Active or inactive uveitis with any treatment status (current / prior / none \[but under surveillance\]).
You may not qualify if:
- Bilateral uveitis with differing etiologies
- Traumatic uveitis
- Post-operative uveitis
- Immediate family member (spouse, biological or legal guardian, child, sibling, parent) who is an investigative site personnel directly affiliated with this study or who is an employee of JAEB Center for Health Research.
- Ocular disease related to Retinoblastoma, Coat's disease, retinitis pigmentosa, inherited retinal degeneration, Juvenile xanthogranuloma (JXG), or leukemia/malignancy within the eye.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (4)
Department of Ophthalmology, Boston University School of Medicine
Boston, Massachusetts, 02118, United States
Akron Children's Hospital
Akron, Ohio, 44308, United States
Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, 45229, United States
Pediatric Ophthalmology Associates, Inc.
Columbus, Ohio, 43205, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Kara C LaMattina, MD
Department of Ophthalmology, Boston University School of Medicine
- STUDY CHAIR
Virginia Miraldi Utz, MD
Children's Hospital Medical Center, Cincinnati
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 12 Months
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 1, 2026
First Posted
April 8, 2026
Study Start
April 14, 2026
Primary Completion (Estimated)
April 1, 2027
Study Completion (Estimated)
April 1, 2028
Last Updated
May 8, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF