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Multicentre, Double-Blind, Randomised, Sham-Controlled Trial of 10 Khz High-Frequency Spinal Cord Stimulation for Chronic Neuropathic Low Back Pain (MODULATE-LBP): a Trial Protocol.

Trials(2020)SCI 4区

Pain Management & Neuromodulation Centre | Guys & St. Thomas NHS Foundation Trust | Institute of Health and Well Being | Wessex Institute | South Tees Hospitals NHS Foundation Trust | Department of Psychology | Univ Liverpool | University of Oxford

Cited 16|Views58
Abstract
Introduction Chronic neuropathic low back pain (CNLBP) is a debilitating condition in which established medical treatments seldom alleviate symptoms. There is evidence demonstrating high frequency 10kHz spinal cord stimulation (SCS) reduces pain and improves health-related quality of life in patients with Failed Back Surgery Syndrome (FBSS) but there is limited evidence in CNLBP without prior surgery. The aim of this multicentre randomised trial is to assess the clinical and cost-effectiveness of 10kHz SCS for this population. Methods This is a multicentre double-blind randomised sham-controlled trial with a parallel economic evaluation. A total of 96 patients with CNLBP who have not had spinal surgery will be implanted with an epidural lead and a sham lead outside the epidural space without a screening trial. Patients will be randomised 1:1 to 10kHz SCS plus usual care (intervention group) or sham 10kHz SCS plus usual care (control group) after full implant. The SCS devices will be programmed identically using a cathodal cascade. Participants will use their handheld programmer to alter the intensity of the stimulation as per routine practice. Primary outcome will be a 7 day daily pain diary. Secondary outcomes include the Oswestry Disability Index, complications, EQ-5D-5L, and health and social care costs. Outcomes will be assessed at baseline (pre-randomisation) and at 1 month, 3 months and 6 months after device activation. The primary analyses will compare primary and secondary outcomes between groups at 6-months adjusting for baseline outcome scores. Incremental cost per quality adjusted life year (QALY) will be calculated at 6-months and over the patient lifetime. Discussion The outcomes of this trial will inform clinical practice and healthcare policy on the role of high frequency 10kHz SCS for patients with CNLBP without prior surgery.
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Spinal cord stimulation,Neuropathic pain,Chronic neuropathic low back pain,Neuromodulation
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要点】:本研究是一项多中心、双盲、随机、假对照试验,旨在评估10kHz高频脊髓刺激对未经手术的慢性神经性腰痛患者的临床和成本效益。

方法】:通过多中心、双盲、随机、假对照试验,将96名未经 spinal 手术的 CNLBP 患者随机分为10kHz SCS 加常规护理(干预组)和假10kHz SCS 加常规护理(对照组)。

实验】:患者在植入 epidural lead 和 sham lead 后,使用手持编程器调节刺激强度,主要结局为7天每日疼痛日记,次要结局包括Oswestry残障指数、并发症、EQ-5D-5L 和健康及社会护理成本。数据将在基线(随机前)及设备激活后1个月、3个月和6个月进行评估。主要分析将比较6个月时两组的主要和次要结局,并计算6个月及患者生命周期内的增量成本效益比。