All patients continue treatment according to the treatment group they were allocated to at the beginning of the BeSt trial. All treatment adjustments will continue to be based on threemonthly DAS measurements, aiming at DAS =<2.4 (or <1.6 before medication may be stopped altogether).
Conditions
Interventions
Continued treatment with established antirheumatic drugs according to accepted treatment strategies, with threemonthly treatment adjustments dictated by the height of the DAS: if DAS>2.4, than medicat
Sponsors
Schering-Plough
Centocor
Eligibility
Inclusion criteria
Inclusion criteria: All patients who completed participation in the first 2 years of BeSt.
Exclusion criteria
Exclusion criteria: N/A
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Functional ability as measured by HAQ; 2. Radiological damage as measured by Sharp/van der Heijde score of hands and feet; 3. Side effects and extra-articular manifestations (as reported and as monitored through laboratory assessments, X-rays, DEXAs). | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Quality of life; 2. Utilities; 3. Work participation; 4. Costs. | — |
Contacts
Public ContactC.F. Allaart
Leiden University Medical Center (LUMC), Department of Rheumatology, C1-39, P.O. Box 9600
Outcome results
None listed