The Parker Institute, Copenhagen University Hospital Bispebjerg Frederiksberg, Copenhagen, Denmark.
Research Unit of Rheumatology, Department of Clinical Research, University of Southern Denmark, Odense University Hospital, Odense, Denmark.
Ann Rheum Dis. 2022 Apr;81(4):537-543. doi: 10.1136/annrheumdis-2021-221129. Epub 2021 Nov 29.
To compare the efficacy of an exercise and education programme with open-label placebo given as intra-articular injections of inert saline on pain and function in individuals with knee osteoarthritis (OA).
In this open-label, randomised controlled trial, we recruited adults aged ≥50 years with symptomatic and radiographically confirmed knee OA in Denmark. Participants were randomised 1:1 to undergo an 8-week exercise and education programme or four intra-articular saline injections over 8 weeks. Primary outcome was change from baseline to week 9 in the Knee Injury and Osteoarthritis Outcome Score (KOOS) questionnaire pain subscale (range 0 (worst)-100 (best)). Prespecified equivalence margins of ±8 KOOS pain points were chosen for the demonstration of comparable efficacy. Key secondary outcomes were the KOOS function and quality of life subscales, and patients' global assessment of disease impact.
206 adults were randomly assigned: 102 to exercise and education and 104 to intra-articular saline injections. For the primary outcome, the least squares mean changes in KOOS pain were 10.0 for exercise and education and 7.3 for saline injections (difference 2.7 points, 95% CI -0.6 to 6.0; test for equivalence p=0.0008). All group differences in the key secondary outcomes respected the predefined equivalence margins. Adverse events and serious adverse events were similar in the two groups.
In individuals with knee OA, an 8-week exercise and education programme provided efficacy for symptomatic and functional improvements equivalent to that of four open-label intra-articular saline injections over 8 weeks.
NCT03843931.
比较运动和教育计划与作为关节内注射惰性盐水的开放性安慰剂在膝骨关节炎(OA)患者中的疼痛和功能疗效。
在这项开放性、随机对照试验中,我们招募了丹麦年龄≥50 岁、有症状和放射学证实的膝 OA 患者。参与者按 1:1 随机分为 8 周的运动和教育计划组或 8 周内 4 次关节内盐水注射组。主要结局是从基线到第 9 周的膝关节损伤和骨关节炎结果评分(KOOS)问卷疼痛子量表的变化(范围 0(最差)-100(最佳))。选择了±8 KOOS 疼痛点的预设等效边界来证明等效疗效。主要次要结局是 KOOS 功能和生活质量子量表以及患者对疾病影响的总体评估。
206 名成年人被随机分配:102 人接受运动和教育,104 人接受关节内盐水注射。对于主要结局,运动和教育的 KOOS 疼痛最小平方均值变化为 10.0,盐水注射为 7.3(差值 2.7 分,95%CI -0.6 至 6.0;等效性检验 p=0.0008)。两组在关键次要结局的所有差异都符合预先设定的等效边界。两组的不良事件和严重不良事件相似。
在膝骨关节炎患者中,8 周的运动和教育计划在症状和功能改善方面的疗效与 8 周内 4 次开放性关节内盐水注射相当。
NCT03843931。