L92.0 L92.1 D86.3
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Presence of a chronic, non-infectious granulomatous skin disease - Treatment with a topical JAK inhibitor (ruxolitinib or delgocitinib) - Treatment duration of at least 4 weeks - Application twice daily, as discussed with the patient
Exclusion criteria
Exclusion criteria: - Evidence that the patients objected to the use of their data for research purposes at any point during the study. - Treatment duration of less than 4 weeks or lack of compliance with the treatment regimen as documented in the medical history
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| - Disease-specific outcomes following treatment with topical JAK inhibitors, as determined by disease-specific scoring systems (absolute and relative changes during treatment) over a maximum of 12 weeks - Granuloma Annulare Severity Index (GASI) - Cutaneous Sarcoidosis Activity and Morphology Instrument (CSAMI) - Necrobiosis Lipoidica Investigator Global Assessment (NL-IGA) and Necrobiosis Lipoidica Lesion Score (NLLS) - Proportion of responders (at least 50% improvement in the respective disease-specific score during treatment) vs. non-responders (less than 50% improvement in the respective disease-specific score during treatment and/or discontinuation or change of therapy due to lack of efficacy by the investigator and/or patient) | — |
Secondary
| Measure | Time frame |
|---|---|
| - Patient satisfaction following treatment with topical JAK inhibitors, as measured by the Dermatology Life Quality Index (DLQI) - Occurrence of side effects - Duration of treatment or time until treatment change or escalation to systemic therapy | — |
Countries
Germany
Contacts
Universitätsklinikum Düsseldorf - Klinik für Dermatologie