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Anti TNF therapy and susceptibility for Coxiella burnetii infection

Anti TNF therapy and susceptibility for Coxiella burnetii infection - Anti TNF therapy and susceptibility for Coxiella burnetii infection

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON35680
Enrollment
800
Registered
2011-09-06
Start date
2011-12-05
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Coxiella burnetii infection Q fever

Interventions

None listed

Sponsors

Universitair Medisch Centrum Sint Radboud
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • Diagnosis of either rheumatoid arthritis (RA), arthritis psoriatica or bechterew disease • Residence in Q fever endemic area (defined by the Institute for Public Health and Environment (RIVM) as *core area*), as determined by the postal code of their home address. • Signed written informed consent ;For patients on anti-TNF therapy: • Treatment with TNFa blockers either infliximab, etanercept or adalimumab in an adequate dose according to the guidelines • Treatment with TNFa blockers is started before 01-01-2011 ;For patients not receiving anti-TNF therapy: • Treatment with DMARDs • No history of treatment with TNFa blockers

Exclusion criteria

Exclusion criteria: • Age under 18 years • Pregnancy or lactation • Lymphoma, lymphoproliferative syndromes and other hematologic malignancies • Chronic infections, including HIV, hepatitis B or C, mycobacterial disease

Design outcomes

Primary

MeasureTime frame
Serology indicative of chronic Q fever or past Q fever infection. In-vitro cytokine production and/or monocyte/macrophage polarisation. The presence of genetic polymorphisms in genes involved in the innate immunity.

Secondary

MeasureTime frame
geen

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)