Multicenter, Interdisciplinary National VEXAS Registry With Accompanying Biomaterial Colle
The aim is rapid collection of real-life data on the epidemiology, treatment and disease course in patients with VEXAS syndrome during routine clinical practice and collect biomaterials to evaluate genotype-phenotype associations, determine optimal treatment schedule, identify diagnostic features and biomarkers
| Condition(s) | VEXAS Syndrome |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Summary | The aim is rapid collection of real-life data on the epidemiology, treatment and disease course in patients with VEXAS syndrome during routine clinical practice and collect biomaterials to evaluate genotype-phenotype associations, determine optimal treatment schedule, identify diagnostic features and biomarkers |
| Who can participate | Inclusion Criteria: * Patients with established or suspected (clinical and hematological criteria) VEXAS Syndrome * Age ≥18 years * Signed informed consent form Exclusion Criteria: * patients who are not in a position to understand the nature and scope of participation in this register |
| Ages | 18 Years |
| Sex | All |
| Lead sponsor | Technische Universität Dresden |
| Locations | Aachen, Germany; Chemnitz, Germany; Dresden, Germany; Düsseldorf, Germany; Essen, Germany; Göttingen, Germany (+11 more sites) |
| Start date | 2024-03-13 |
| NCT ID | NCT06377462 |
| Official listing | https://clinicaltrials.gov/study/NCT06377462 |