Assessment of Wrist Joint and Knee Joint Inflammation in Patients With Rheumatoid Arthritis by Quantitative Three Dimensional Power Doppler... | NCT00858169 | Trialant
CompletedObservationalUpdated Feb 13, 2015
Assessment of Wrist Joint and Knee Joint Inflammation in Patients With Rheumatoid Arthritis by Quantitative Three Dimensional Power Doppler Ultrasonography
Taichung Veterans General Hospital
ClinicalTrials.gov ID
NCT00858169
Lead Sponsor
Taichung Veterans General HospitalOTHER
Overall Status
Completed
Study Type
Observational
Enrollment
49Actual
Last Update Posted
Feb 13, 2015Estimated
Start Date
Mar 2009
Primary Completion Date
Mar 2010Actual
Completion Date
Mar 2010Actual
Official Title
Taichung Veterans General Hospital
Brief Summary
The purpose of this study is to:
To investigate the wrist joint synovial blood flow intensity and model by quantitative three-dimensional (3D) power Doppler ultrasonography (PDUS) in patients with rheumatoid arthritis before and after initiation of a new medicine and compare these data with routinely used clinical data and laboratory findings, such as pain score, erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP)
To investigate the intra-observer and inter-observer agreement of quantitative 3D PDUS assessment of the vascularity in wrist joints and knee joints using automatic volume scan.
Rheumatoid Arthritis
No interventions
There are no interventions for this study.
Ages Eligible for Study
Child (0-17)Adult (18-64)Older Adult (65+)
Sexes Eligible for Study
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients who fulfill the 1987 ARA criteria for RA
Patients with at least one painful swollen wrist or knee joint observed by a rheumatologist
Patients who will receive a new medicine, including oral corticosteroid, intravenous methylprednisolone pulse therapy, intraarticular injection with steroid or methotrexate, DMARDs, or biologic agent
Exclusion Criteria:
Patients with active infection
Patients with concurrent malignant disease
Patients with a history of traumatic, septic, or cystal arthritis, previous joint surgery, or arthroscopic synovectomy of any wrist or kneejoint within the past 12 months before the study
Patients who have severe wrist or knee joint deformity that makes the US assessment protocol unable to complete