MRI引导聚焦超声(MRgFUS)治疗局灶性手肌张力障碍的疗效和安全性评估:一项开放标签非随机临床试验的研究方案。

IF 2.1 Q3 CLINICAL NEUROLOGY
BMJ Neurology Open Pub Date : 2023-10-25 eCollection Date: 2023-01-01 DOI:10.1136/bmjno-2023-000522
Joel Maamary, James Peters, Kain Kyle, Diane Ruge, Benjamin Jonker, Yael Barnett, Stephen Tisch
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引用次数: 0

摘要

简介:MRI引导聚焦超声(MRgFUS)丘脑切除术在微创立体定向神经外科领域取得了令人兴奋的进展。目前对局灶性手肌张力障碍的治疗选择有限,很少使用可能更有效的侵入性立体定向干预措施,如脑深部刺激或病变治疗。微创脑损伤的出现提供了一种潜在的安全有效的治疗方法,最近的一项试点研究将MRgFUS-Vo复合丘脑切除术确立为局灶性手肌张力障碍的有效治疗选择。在这项研究中,我们进行了一项开放标签临床试验,以进一步确定MRgFUS-Vo复合体丘脑切开术是治疗局灶性手肌张力障碍的有效方法,并更加关注与该治疗相关的潜在运动成本。为了阐明肌张力障碍的病理生理学和治疗机制,将纵向进行神经生理学和MRI分析,以探索可能成为这种治疗益处基础的神经可塑性和结构变化的假设。方法和分析:共有10名参与者将被招募到这项开放标签临床试验中。所有参与者将在基线时接受临床、运动测量、神经生理学和放射学测试,然后在MRgFUS-Vo复杂丘脑切除术后预先指定的时间点进行重复测量。此外,为了确定局灶性手肌张力障碍患者存在的任何潜在结构或神经生理学异常,将招募10名年龄和性别匹配的对照参与者进行比较研究。这些结果将在基线和12个月时与干预参与者进行比较,以评估这些异常的正常化(如果存在)。伦理和传播:该试验由圣文森特健康网络悉尼人类研究伦理委员会审查并批准(2022/ETH00778)。研究结果将发表在同行评审期刊上,并在国家和国际会议上发表。试验注册号:CTRN126222000775718。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluation of the efficacy and safety of MRI-guided focused ultrasound (MRgFUS) for focal hand dystonia: study protocol for an open-label non-randomised clinical trial.

Evaluation of the efficacy and safety of MRI-guided focused ultrasound (MRgFUS) for focal hand dystonia: study protocol for an open-label non-randomised clinical trial.

Introduction: MRI-guided focused ultrasound (MRgFUS) thalamotomy provides an exciting development in the field of minimally invasive stereotactic neurosurgery. Current treatment options for focal hand dystonia are limited, with potentially more effective invasive stereotactic interventions, such as deep brain stimulation or lesional therapies, rarely used. The advent of minimally invasive brain lesioning provides a potentially safe and effective treatment approach with a recent pilot study establishing MRgFUS Vo-complex thalamotomy as an effective treatment option for focal hand dystonia. In this study, we undertake an open-label clinical trial to further establish MRgFUS Vo-complex thalamotomy as an effective treatment for focal hand dystonia with greater attention paid to potential motor costs associated with this treatment. To elucidate pathophysiology of dystonia and treatment mechanisms, neurophysiological and MRI analysis will be performed longitudinally to explore the hypothesis that neuroplastic and structural changes that may underlie this treatment benefit.

Methods and analysis: A total of 10 participants will be recruited into this open-label clinical trial. All participants will undergo clinical, kinemetric, neurophysiological and radiological testing at baseline, followed by repeated measures at predesignated time points post MRgFUS Vo-complex thalamotomy. Further, to identify any underlying structural or neurophysiological abnormalities present in individuals with focal hand dystonia, 10 age and gender matched control participants will be recruited to undergo comparative investigation. These results will be compared with the intervention participants both at baseline and at 12 months to assess for normalisation of these abnormalities, if present.

Ethics and dissemination: This trial was reviewed and approved by the St Vincent's Health Network Sydney Human Research Ethics Committee (2022/ETH00778). Study results will be published in peer-reviewed journals and presented at both national and international conferences.

Trial registration number: CTRN12622000775718.

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来源期刊
BMJ Neurology Open
BMJ Neurology Open Medicine-Neurology (clinical)
CiteScore
3.20
自引率
3.70%
发文量
46
审稿时长
13 weeks
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