anterior and/or intermediate and/or posterior uveitis
Conditions
Interventions
None listed
Sponsors
Academisch Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Age *18 years Diagnosed with uveitis Mentally competent
Exclusion criteria
Exclusion criteria: Patients who do not speak or understand the Dutch language will be excluded from participation in this study. Age *18 years Patients with a family history of retinal dystrophy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The retinal function measured by ERG is the main outcome of the study. ERG reduction, reflecting retinal damage, will be analysed throughout the course of uveitis. ERGs will be evaluated on several parameters, including a and b wave amplitude, latency, waveform, b:a wave ratio, and oscillatory potentials. | — |
Secondary
| Measure | Time frame |
|---|---|
| - When ERG reduction, reflecting retinal damage, occurs in the course of uveitis. - To which extent different forms of uveitis, i.e. anterior, intermediate, posterior, panuveitis or specific diagnosis influence ERG abnormalities - To which extent clinical parameters, including demographics, treatment and ophthalmologic examination results (e.g. visual acuity, severity of inflammation scored according to the SUN criteria18, flare, presence of CME, retinal vasculitis or chorioiditis on FA, OCT values and visual fields) influence ERG abnormalities. - To which extent ERG abnormalities are reversible. | — |
Countries
Netherlands
Outcome results
None listed