H46 G35 G36.0
Conditions
Interventions
Group 1: The following data will be collected on a study basis: Medical history, questionnaires on affective disorders (BDI-II) and on visual quality of life (NEI-VFQ-25 with neurovisual supplement),
Sponsors
Experimental and Clinical Research Center (ECRC), AG Klinische Neuroimmunologie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Diagnosis of acute optic neuritis - 18 years and older - Person capable of giving consent - Person has health insurance (for clarification of possible incidental findings) - Written consent to participate in the present study
Exclusion criteria
Exclusion criteria: Pregnancy at study inclusion, Relevant concomitant condition considered limiting to study feasibility (e.g., reduced general health due to comorbidities, obesity per magna, acute need for treatment for mental illness, dementia-related syndrome), Insufficient ability to cooperate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The aim of the data collection is a prospective follow-up of patients with acute optic neuritis. | — |
Secondary
| Measure | Time frame |
|---|---|
| Descriptive characterization of acute optic neuritis of different etiology and its course during the observation period, both at the level of structural tissue changes, at the level of immunological functions, at the level of symptoms and function, and at the level of subjective effects and possible modifiers of disease progression. | — |
Countries
Germany
Contacts
Public ContactSusanna Asseyer
Experimental and Clinical Research Center (ECRC), AG Klinische Neuroimmunologie
Outcome results
None listed