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Tumor Necrosis Factor blockade in patients with Rheumatoid Arthritis inhibits Atherothrombosis.

Tumor Necrosis Factor blockade in patients with Rheumatoid Arthritis inhibits Atherothrombosis.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON29079
Enrollment
15
Registered
2006-12-12
Start date
2006-01-01
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

Rheumatoid Arthritis

Interventions

TNF-alpha blockade. (patients are their own control)

Sponsors

Academic Medical Center Amsterdam, the Netherlands
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male or female patients who were priorly diagnosed with RA, who are currently experiencing an inflammatory episode and who will be treated with TNF-alpha blockade; 2. Age 18-80 years.

Exclusion criteria

Exclusion criteria: 1. Patients who were priorly diagnosed with diabetes, hypertension or cardiovascular disease; 2. Current signs or symptoms of severe, progressive or uncontrolled hepatic, haematological, gastroenterological, endocrine, pulmonary, cardiac or neurological disease.

Design outcomes

Primary

MeasureTime frame
1. Endothelial Function (FMD); 2. Glycocalyx; Before treatment, 0-4 weeks after treatment, 9-12 weeks after treatment.

Secondary

MeasureTime frame
1. Atherosclerosis: Plasma: Total cholesterol, LDL, HDL, Triglycerides, Lp(a), ox-LDL; 2. Thrombosis: D-dimer, F1+2, sTF, PAI-I; 3. Inflammation: IL-1beta, TNF-alpha, IL-6, IL-8, IL-10, hsCRP. Before treatment, 0-4 weeks after treatment, 9-12 weeks after treatment.

Contacts

Public ContactSander Leuven, van

Academic Medical Center (AMC), Department of Vascular Medicine, room F4-159.2, P.O. Box 22660

s.i.vanleuven@amc.uva.nl+31 (0)20 5668675

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)