McLachlan Hanan, Maher Christopher G, Lin Chung-Wei Christine, Billot Laurent, Day Richard O, Ivers Rowena, Underwood Martin, McLachlan Andrew J, Richards Bethan, Finnerup Nanna B, Ferreira Giovanni E
Institute for Musculoskeletal Health, Sydney Local Health District, Sydney, New South Wales, Australia
Sydney School of Public Health, Faculty of Medicine and Health, The University of Sydney, Sydney, New South Wales, Australia.
BMJ Open. 2024 Dec 31;14(12):e096796. doi: 10.1136/bmjopen-2024-096796.
Sciatica is a debilitating condition that often becomes chronic, and for which there are few effective treatment options. Treatments such as the anti-depressant duloxetine have shown promise, but the evidence is inconclusive. We are describing a high quality, definitive trial to investigate the efficacy, safety and cost-effectiveness of duloxetine in chronic sciatica.
The duloxetine for chronic sciatica (DREAM) trial is a randomised, superiority, parallel-group, placebo-controlled, triple-blinded (participant, clinician, assessor) trial with an adaptive group sequential design investigating the efficacy and safety of duloxetine in participants with chronic sciatica of at least 3 months duration. Participants will be randomised at a 1:1 ratio to duloxetine or placebo. 332 participants will be recruited on presentation to general practices, specialist clinics and hospital emergency departments or from hospital in-patient wards and from the community. In the active treatment group, participants will receive duloxetine 60 mg per day for 12 weeks, including 1 week of titration at 30 mg/day. The treatment phase will be followed by a 2-week tapering phase where they will receive duloxetine 30 mg/day. Participants will be followed-up for 1 year, with outcomes being measured 4, 8, 12, 16, 26, and 52 weeks post-randomisation. The primary outcome is leg pain intensity at 12 weeks post-randomisation. Secondary outcomes include back pain intensity, disability, time to recovery, quality of life, depressive and anxiety symptoms, and sleep disturbance. Adverse events will be recorded, and a cost-effectiveness analysis will be conducted.
Ethical approval has been granted by the University of Sydney Human Research Ethics Committee. Trial results will be disseminated by publications, conference presentations and via the media.
ACTRN12624000919516.
坐骨神经痛是一种使人衰弱的病症,常常会变成慢性疾病,而针对这种疾病几乎没有有效的治疗选择。像抗抑郁药度洛西汀这样的治疗方法已显示出一定前景,但证据并不确凿。我们正在描述一项高质量的确定性试验,以研究度洛西汀治疗慢性坐骨神经痛的疗效、安全性和成本效益。
度洛西汀治疗慢性坐骨神经痛(DREAM)试验是一项随机、优效性、平行组、安慰剂对照、三盲(参与者、临床医生、评估者)试验,采用适应性组序设计,研究度洛西汀对病程至少3个月的慢性坐骨神经痛患者的疗效和安全性。参与者将按1:1的比例随机分为度洛西汀组或安慰剂组。将从全科诊所、专科诊所、医院急诊科、医院住院病房或社区招募332名参与者。在活性治疗组中,参与者将每天服用60毫克度洛西汀,持续12周,包括以每天30毫克的剂量进行1周的滴定期。治疗阶段之后是为期2周的减量期,在此期间他们将每天服用30毫克度洛西汀。参与者将接受为期1年的随访,在随机分组后的第4、8、12、16、26和52周测量结果。主要结局是随机分组后12周时的腿部疼痛强度。次要结局包括背痛强度、残疾情况、恢复时间、生活质量、抑郁和焦虑症状以及睡眠障碍。将记录不良事件,并进行成本效益分析。
悉尼大学人类研究伦理委员会已批准该试验的伦理申请。试验结果将通过出版物、会议报告和媒体进行传播。
ACTRN12624000919516。