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动态振荡刺激用于慢性偏头痛的预防性治疗:一项随机、双盲、假对照试验

Kinetic Oscillation Stimulation for the Preventive Treatment of Chronic Migraine: A Randomized, Double-Blind, Sham-Controlled Trial.

作者信息

Hoffmann Jan, Kaube Holger, Rimmele Florian, Jürgens Tim P, Nissilä Markku, Gaul Charly, Kallela Mikko, Keski-Säntti Petra, Sumelahti Marja-Liisa, Straube Andreas, Lewis David, Hoffmann Vanessa, Wirtz Larissa, Rempel Annette, Böhm Olaf, May Arne

机构信息

Wolfson Sensory, Pain and Regeneration Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, United Kingdom.

NIHR-Wellcome Trust King's Clinical Research Facility/SLaM Biomedical Research Centre, King's College Hospital, United Kingdom.

出版信息

Neurology. 2025 Feb 11;104(3):e210220. doi: 10.1212/WNL.0000000000210220. Epub 2025 Jan 9.

Abstract

BACKGROUND AND OBJECTIVES

The Chordate System administers kinetic oscillation stimulation (K.O.S) into the nasal cavity thereby potentially modulating the activity of trigemino-autonomic reflex. Modulation of this reflex has been proposed as a potential therapeutic target in migraine. The aim of this clinical trial was to evaluate the efficacy of K.O.S for the preventive treatment of chronic migraine (CM).

METHODS

In this randomized, double-blind, sham-controlled, multicenter clinical trial, patients with CM were treated with K.O.S once per week over a period of 6 weeks. The primary performance endpoint was the mean change in monthly headache days with moderate to severe intensity (MHDs) from the 28-day pretreatment baseline period to the performance assessment period (days 14-42 of treatment). Mean change from baseline in monthly migraine days (MMDs), proportion of participants with 30% and 50% or greater reduction in moderate to severe headache days compared with baseline, and change in the use of abortive medications from baseline were also assessed during the performance assessment period. Headache-related disability and quality-of-life measures were evaluated up to 70-day posttreatment.

RESULTS

The primary endpoint showed a significantly larger reduction of MHD across the performance assessment period with active treatment (-3.5 days, n = 67) compared with sham (-1.2 days, n = 65) ( = 0.0132). Compared with sham, active treatment consistently also led to significant reduction of MHD during the follow-up period (-2.7 [-4.3; -1.0, = 0.0014]) as well as of mean MMDs during the assessment (-2.4 [-4.1; -0.7, = 0.0048]) and follow-up (-2.9 [-4.5; -1.2, = 0.0008]) periods. 61.8% of participants reported treatment-emergent adverse events (TEAEs) with similar incidences among treatment groups (63.2% [active], 60.3% [sham]), with nasopharyngitis (8.3%), dizziness (6.3%), and epistaxis (6.3%) being the most common TEAEs. Treatment-related serious adverse events were not observed.

DISCUSSION

The Chordate System provides significant benefits to patients with CM by reducing the number of MHDs. The nonpharmacologic nature of the treatment option positions K.O.S as a valuable addition to the current therapeutic portfolio for the management of CM.

TRIAL REGISTRATION INFORMATION

The trial was registered on ClinicalTrials.gov (NCT03400059) on January 17, 2018. The first patient was enrolled on March 22, 2018, and the last patient completed the study on October 1, 2022. The trial registration initially described the timing of the secondary endpoints incorrectly due to clerical error, and this was corrected to match the protocol and analysis plan once discovered.

CLASSIFICATION OF EVIDENCE

This study provides Class I evidence that weekly intranasal K.O.S is associated with a reduced number of headache days per month in patients with CM.

摘要

背景与目的

脊索系统对鼻腔进行动态振荡刺激(K.O.S),从而可能调节三叉神经自主反射的活动。这种反射的调节已被提议作为偏头痛的一个潜在治疗靶点。本临床试验的目的是评估K.O.S预防慢性偏头痛(CM)的疗效。

方法

在这项随机、双盲、假对照、多中心临床试验中,CM患者接受为期6周、每周一次的K.O.S治疗。主要疗效终点是从28天的治疗前基线期到疗效评估期(治疗的第14 - 42天),每月中重度强度头痛天数(MHDs)的平均变化。在疗效评估期内,还评估了每月偏头痛天数(MMDs)相对于基线的平均变化、与基线相比中重度头痛天数减少30%和50%或更多的参与者比例,以及急救药物使用量相对于基线的变化。在治疗后长达70天的时间里评估与头痛相关的残疾和生活质量指标。

结果

主要终点显示,在整个疗效评估期内,与假治疗组(-1.2天,n = 65)相比,积极治疗组(-3.5天,n = 67)的MHDs减少幅度显著更大(P = 0.0132)。与假治疗组相比,积极治疗在随访期内也持续导致MHDs显著减少(-2.7 [-4.3;-1.0],P = 0.0014),以及在评估期(-2.4 [-4.1;-0.7],P = 0.0048)和随访期(-2.9 [-4.5;-1.2],P = 0.0008)内MMDs显著减少。61.8%的参与者报告了治疗中出现的不良事件(TEAEs),各治疗组发生率相似(积极治疗组63.2%,假治疗组60.3%),最常见的TEAEs为鼻咽炎(8.3%)、头晕(6.3%)和鼻出血(6.3%)。未观察到与治疗相关的严重不良事件。

讨论

脊索系统通过减少MHDs数量为CM患者带来显著益处。该治疗方案的非药物性质使K.O.S成为CM管理当前治疗组合中有价值的补充。

试验注册信息

该试验于2018年1月17日在ClinicalTrials.gov(NCT03400059)注册。首例患者于2018年3月22日入组,最后一例患者于2022年10月1日完成研究。由于文书错误,试验注册最初对次要终点的时间描述有误,一经发现即进行了更正,以使其与方案和分析计划一致。

证据分级

本研究提供了I类证据,表明每周一次的鼻内K.O.S与CM患者每月头痛天数减少相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93f0/11720095/cc61a3dd90c9/WNL-2023-005486f1.jpg

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