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N/A N=90 Randomized Treatment

Intra-articular Glucocorticoid Treatment of the Elbow

Rheumatoid Arthritis

Enrolled (actual)
90
Serious AEs
0.0%
Results posted
Nov 2009
Primary outcome: Primary: Relapse of Arthritis — 8; 13; 44; 46 participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
immobilisation in a triangular sling (Behavioral)
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
Region Gävleborg
Primary completion
Dec 2008

Outcome Measures

OutcomeResultp-value
PRIMARY
Relapse of Arthritis
8; 13; 44; 46; 43; 43

Summary

BACKGROUND: Intra-articular glucocorticoid injections are frequently used to relieve symptoms of arthritis. Postinjection rest has been shown to improve the outcome of knee joint injections, but not for wrist injections. Consequently, different joints respond differently on postinjection regimens. OBJECTIVES: To investigate whether better treatment results might be achieved of post-injection rest following intra-articular glucocorticoid treatment for elbow synovitis. METHODS: 90 patients with rheumatoid arthritis (RA) and elbow synovitis were treated with 20 mg intra-articular triamcinolone hexacetonide and randomised to either a 48 hour immobilisation in a triangular sling (n=46) or normal activity without restrictions (n=44). Primary endpoint was relapse of synovitis. In addition, pain, function according to a self assessment questionnaire (PREE) and range of movement were followed for six months.

Eligibility Criteria

Inclusion Criteria

  • Rheumatoid arthritis, and
  • Clinical signs of elbow synovitis

Exclusion Criteria

  • Patients in function class 4 according to Steinbrocker as well as patients with oral glucocorticoid treatment corresponding to more than 7.5 mg prednisolone or intra-articular treatment in the joint the past three months
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00972530). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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