Skip to main content
Clinical Trials/ISRCTN75459849
ISRCTN75459849
Completed
Not Applicable

A randomised, double-blinded, controlled trial of ultrasound guided and conventional clinical examination guided intra-articular corticosteroid injection of large and medium synovial joints in inflammation arthritis

ewcastle Hospitals NHS Trust (UK)0 sites240 target enrollmentJanuary 26, 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
All inflammatory arthritidies
Sponsor
ewcastle Hospitals NHS Trust (UK)
Enrollment
240
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 26, 2007
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional

Investigators

Sponsor
ewcastle Hospitals NHS Trust (UK)

Eligibility Criteria

Inclusion Criteria

  • 1\. Patients who fulfil the American Rheumatology Association (ARA) Criteria for Rheumatoid Arthritis (RA) or have an established diagnosis of inflammatory arthritis
  • 2\. Age greater than 16 years
  • 3\. Presentation with an exacerbation of pain and/or stiffness and/or local findings of synovitis (at least two out of the three) of one of either the shoulder, elbow, wrist, knee or ankle joint (hip is excluded as we believe it should only be injected with imaging guidance)
  • 4\. Patients must be able to comply with the protocol and give their written informed consent to participate

Exclusion Criteria

  • 1\. Radiological evidence of severe joint disease as assessed by previous x\-ray of the affected joint
  • 2\. Patients receiving treatment for RA and not stabilised on Non\-Steroidal Anti\-Inflammatory Drugs (NSAIDs), Disease Modifying Anti\-Rheumatic Drugs (DMARDs) and/or corticosteroid therapy for one month or longer
  • 3\. Evidence of co\-existent sepsis
  • 4\. A second joint requiring immediate corticosteroid injection
  • 5\. An acute flare of RA deemed severe enough by the patient?s supervising clinician to require an alteration in DMARD therapy
  • 6\. Use of intra\-articular or intra\-muscular steroids in the 28 days prior to study entry
  • 7\. Allergy to corticosteroids or contrast material

Outcomes

Primary Outcomes

Not specified

Similar Trials