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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 arthritis
Synovitis and vascularization by use of ultrasonography including power Doppler
Inflammatory and Immune System - Rheumatoid arthritis
Musculoskeletal - 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
NameTimeMethod
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
NameTimeMethod
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]
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