MedPath

Clinical Outcome in Uveitis

Completed
Conditions
Uveitis
Registration Number
NCT01983488
Lead Sponsor
Moorfields Eye Hospital NHS Foundation Trust
Brief Summary

This study is aimed at investigating the long term clinical outcome of patients with uveitis.

Detailed Description

Patients will be included if they are treated for uveitis and have had repeat follow-up. Data will be gathered from the entire length of the patients follow-up.

The main outcome measures will be:

Change from baseline of Best corrected visual acuity (BCVA)at 10 years Causes of vision loss (≤6/15, VL) and severe vision loss (≤6/60, SVL) at 10 years Number of clinical visits at 10 years.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
231
Inclusion Criteria
  • Clinical Diagnosis of Uveitis.
Exclusion Criteria
  • No follow-up data.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Best Corrected Visual Acuityup to 10 years

Recorded repeat best corrected visual acuity at intervals throughout the length of follow-up.

Secondary Outcome Measures
NameTimeMethod
Causes of visual lossFirst follow-up, years 1,2,5,10, Final follow-up

Record any ocular changes related to permanent visual loss under 6/12 and severe visual loss under 6/60.

Trial Locations

Locations (1)

Moorfields Eye Hospital

🇬🇧

London, United Kingdom

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