A longitudinal study of patients with rheumatoid arthritis starting biological therapy; Assessment of joint inflammation by use of ultrasonography
Not Applicable
Completed
- Conditions
- Arthritis in patients with rheumatoid arthritisSynovitis and vascularization by use of ultrasonography including power DopplerInflammatory and Immune System - Rheumatoid arthritisMusculoskeletal - Other muscular and skeletal disorders
- Registration Number
- ACTRN12610000284066
- Lead Sponsor
- Abbott Norge AS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 296
Inclusion Criteria
Patients with rheumatoid arthritis
Clinical indication for starting biological treatment
Exclusion Criteria
Not prosthesis in more than 5 of the joints examined by ultrasonography.
Not enough knowledge of the Norwegian language to answer questionnaires.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess whether ultrasonographic examination of 36 joints and 4 tendons will be able to indicate responders to biological medication earlier than regular assessments (clinical and laboratory)[ Assessments at baseline and after 1, 2, 3, 6 and 12 months.]
- Secondary Outcome Measures
Name Time Method Degree of power Doppler activity at baseline and radiographic detorioration (hands and feet) after 12 months.[ Baseline power Doppler<br>12 months radiography];Associations between ultrasonographic findings and clinical as well as laboratory assessments.[ Baseline and at 1, 2, 3, 6 and 12 months]