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膝关节骨关节炎患者关节腔内注射透明质酸钠的临床试验

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

作者信息

Dixon A S, Jacoby R K, Berry H, Hamilton E B

机构信息

Royal National Hospital for Rheumatic Diseases, Bath, England.

出版信息

Curr Med Res Opin. 1988;11(4):205-13. doi: 10.1185/03007998809114237.

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 Ten patients (5 of 30 on active treatment; 5 of 33 on placebo) were withdrawn prematurely.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 less than 0.05 to p less than 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 less than 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 less than 0.01) throughout the period from 5 to 23 weeks. The difference between sodium hyaluronate and placebo was significant (p less than 0.05 to p less than 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.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

一项多中心随机、双盲、平行组临床试验在63例膝骨关节炎患者中开展,以比较关节腔内注射20mg透明质酸钠一个疗程与类似疗程的安慰剂注射的疗效和耐受性。治疗包括在23周内进行多达11次注射。在治疗过程中及之后25周,通过主观症状和活动评估进行评价。10例患者(活性治疗组30例中的5例;安慰剂组33例中的5例)提前退出。通过视觉模拟量表(VAS)评估的运动疼痛显示,在使用透明质酸钠治疗的前11周内,平均评分有统计学意义(p<0.05至p<0.0001)的降低,但安慰剂治疗的降低幅度较小且无统计学意义。治疗之间的差异在5周时具有统计学意义(p<0.05)。同样通过VAS评估的静息痛显示,安慰剂组平均评分变化不大,但透明质酸钠组在5至23周期间有逐渐降低,且具有统计学意义(p<0.01)。透明质酸钠与安慰剂之间的差异在第5、11、15、19和23周时具有统计学意义(p<0.05至p<0.002)。使用标准量表评估“日常生活活动”。两种治疗均有小幅改善,在一些评估中具有统计学意义,且透明质酸钠组比安慰剂组改善稍大,但两组之间无统计学意义的差异。(摘要截断于250字)

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