Skip to content

Prevalence of clinical characteristics of patients with a (probable) Behçet*s syndrome in the Netherlands, a follow up cohort study.

Prevalence of clinical characteristics of patients with a (probable) Behçet*s syndrome in the Netherlands, a follow up cohort study. - Behcet study, longitudinal follow up

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON45634
Enrollment
200
Registered
2017-07-13
Start date
2017-02-03
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Behcet Syndrome Behcet's disease

Interventions

Behcet syndrome
immunology
observational study
questionnaires

Sponsors

Jan van Breemen Instituut
Lead Sponsor

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

MeasureTime frame
No endpoints were defined, since it is an observational cohort study.

Secondary

MeasureTime 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

Source: NL-OMON (via WHO ICTRP)