Rheumatoid arthritis
Conditions
Interventions
None listed
Sponsors
Academisch Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Men/women suffering from rheumatoid arthritis, based on the 2010 American College of Rheumatology/ European league Against Rheumatism (ACR/EULAR) classification criteria for RA will be included in this study.;Patients in ARA functional classes I, II, and III may be included.;In addition, patients must fulfill the following criteria at baseline: 1) DAS 28 * 2.6 for the duration of a minimum of 24 weeks 2) Be > 18 years of age and * 85 years. 3) Stable use of concomitant DMARDs and TNF antagonists for the duration of 24 weeks before baseline
Exclusion criteria
Exclusion criteria: 1) The use of oral/ intra-articular corticosteroids within 6 months prior to baseline 2) Pregnancy 3) Breastfeeding 4) Subjects who are impaired, incapacitated, or incapable of completing study related assessments. 5) Subjects who meet diagnostic criteria for any other rheumatic disease (e.g., lupus erythematous). 6) Subjects with active vasculitis of a major organ system with the exception of rheumatoid nodules. 7) Subjects with current symptoms of severe, progressive, or uncontrolled renal, hepatic, hematological, gastrointestinal, pulmonary, cardiac, neurological, or cerebral disease, or other medical conditions that, in the opinion of the investigator, might place the subject at unacceptable risk for participation in this study. 8) Subjects who have clinically significant drug or alcohol abuse. 9) Inability to give informed consent 10) Mental condition rendering the patient unable to understand the na¬ture, scope and possible consequences of the study and/or evidence of an uncooperative attitude.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint of the study is: 1. The percentage of patients that sustain drug-free remission 24 months after the cessation of TNF-antagonists 2. Predictors (e.g. clinical parameters, serological and immunological markers) of sustained drug-free remission | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. The difference in genetic markers/ epigenetic markers (e.g. genetic polymorphisms/ methylation status) in TNF-* genes that predict sustained drug-free remission in the individual patient 2. Explore new markers, e.g. by micro-array analysis, distinguishing patients with sustained drug-free remission from patients who relapse. 3. Determine the percentage of patients with subclinical synovitis as determined by ultrasound in this group of patients in clinical remission | — |
Countries
Netherlands
Outcome results
None listed