REstore Working Ability in RheumatoiD Arthritis
- Sponsor
- The Rheumatological Center of Helsinki
- Study ID
- NCT01405326
- Phase
- PHASE4
- Status
- Unknown
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 25 Years - 55 Years
- Healthy Volunteers
- Not accepted
Interventions
- adalimumab — BIOLOGICAL40mg sc. every two weeks for six months
Study Details
The purpose of the study is to assess whether a 6-month treatment with adalimumab added on the treatment with conventional antirheumatic drugs (DMARD) will decrease the number of days on sick leave compared to placebo. In addition, the cost-effectiveness and cost-utility of the intervention compared to the conventional treatment is evaluated, and the patients who benefit most are characterized.
Key Dates
- Start date
- May 31, 2011
- Status verified
- Jul 2011
- Primary completion
- Dec 31, 2012
- Completion
- Mar 31, 2013
Study Design
- Enrollment
- 160 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
Arms
- Experimental: AdalimumabAdalimumab treatment for 6 months
- Placebo Comparator: PaceboCorresponding placebo for active treatment group
Primary Outcome Measure
Number of lost work days due to RA during the 6-month follow up. [ Time Frame: 6 months ]
Central Contacts
- Kari K Eklund, MD+358405832866
- Kari Puolakka, MD+358408354734
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