Clinical trial of intra-articular injection of sodium hyaluronate in patients with osteoarthritis of the knee

Abstract

A multi-centre randomized, double-blind, parallel-group clinical trial was carried out in 63 patients with osteoarthritis of the knee to compare the efficacy and tolerability of a course of intra-articular injections of 20 mg sodium hyaluronate with a similar course of injections of placebo. Treatment consisted of up to 11 injections over a 23-week period. Evaluation was by means of subjective symptom and activity assessments, serially during the course of treatment and also 25 weeks thereafter. Ten patients (5 of 30 on active treatment; 5 of 33 on placebo) were withdrawn prematurely. Pain on movement, assessed by visual analogue scale (VAS) showed statistically significant (p<0.05 to p<0.0001) reductions in mean scores throughout the first 11 weeks of treatment with sodium hyaluronate but smaller, non-significant, reductions with placebo treatment. The difference between treatments was significant (p<0.05) at 5 weeks. Pain at rest, also assessed by VAS, showed little change in mean scores with placebo but with sodium hyaluronate there was a progressive reduction which was significant (p<0.01) throughout the period from 5 to 23 weeks. The difference between sodium hyaluronate and placebo was significant (p<0.05 to p<0.002) at Weeks 5, 11, 15, 19 and 23. 'Activities of daily living' were assessed using a standard scale. There were small improvements with both treatments, significant at some assessments and somewhat greater with sodium hyaluronate than placebo, but there were no statistically significant differences between the groups. One patient developed a haemarthrosis after sodium hyaluronate injection, which may have been treatment related. Increase in knee effusion volume and the development of phlebitis in 2 other patients were of uncertain relationship to sodium hyaluronate therapy. There were no other reports of local or systemic adverse reactions to sodium hyaluronate therapy and laboratory screening investigations revealed no evidence of toxicity. These results indicate that a course of intra-articular injections of sodium hyaluronate (20 mg) is generally well tolerated in patients with osteoarthritis of the knee and that it results in significant reductions in knee pain in such patients. Further studies should be undertaken to clarify the part that sodium hyaluronate has to play in the management of patients with osteoarthritis of major joints. © 1988 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted.