Behcet Syndrome Behcet's disease
Conditions
Interventions
Behcet syndrome
immunology
observational study
questionnaires
Sponsors
Jan van Breemen Instituut
Eligibility
Age
18 Years to 64 Years
Inclusion criteria
Inclusion criteria: Adult patients who fullfill the international criteria of Behcet syndrome. Those with a clinical suspicion of Behcet syndrome.
Exclusion criteria
Exclusion criteria: none (except no informed consent)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| No endpoints were defined, since it is an observational cohort study. | — |
Secondary
| Measure | Time frame |
|---|---|
| We wil record occurrence of disease manifestations and treatment given. Disease activity and QoL will be assessed using various questionnaires. We will measure NETosis by levels of circulating nucleosomes and systemic neutrophil activation will be assessed by released neutrophil elastase complex with its natural inhibitor alfa1-antitrypsine (ELA complexes) and levels of circulating nucleosomes. T cel regulation will be measured by clonal expansion. | — |
Countries
The Netherlands
Outcome results
None listed