L63.0 L63.1 L63.2 L63.8
Conditions
Interventions
Group 1: Patients 18+ years of age with the definite diagnosis of AA matching the specified clinical subtype / disease stage (AA totalis, AA universalis, Ophiasis, patch-type AA).
Pregnant women and
Sponsors
Medizinische Universität Wien
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Definite diagnosis of alopecia areata with a defined clinical subtype.
Exclusion criteria
Exclusion criteria: Pregnancy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Characterisation of the immune infiltrate in different subtypes of AA and adjacent non-lesional skin. | — |
Secondary
| Measure | Time frame |
|---|---|
| To identify predictive markers (ie. presence of certain immune cells) that can be used to predict therapy response. | — |
Countries
Austria
Contacts
Public ContactJohannes Griss
Medizinische Universität Wien
Outcome results
None listed