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一项2期随机对照、患者与评估者双盲研究的方案:联合皮质和小脑双靶点经颅磁刺激治疗特发性震颤的疗效和安全性

Protocol for a Phase 2 randomized controlled patient-assessor blinded study: efficacy and safety of combined cortical and cerebellar dual-target transcranial magnetic stimulation for the treatment of essential tremor.

作者信息

Xu Jing, Cao Na, Qu Yan, Shang Suhang, Liu Xincheng, Wang Xuexin, Hu Fangfang, Bai Xuerong, Qu Qiumin, Zhang Meng, Cao Hongmei

机构信息

Department of Neurology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

College of Mechanical Engineering, Xi'an Jiaotong University, Xi'an, China.

出版信息

Front Neurol. 2025 Jan 8;15:1505154. doi: 10.3389/fneur.2024.1505154. eCollection 2024.

Abstract

BACKGROUND

Essential tremor (ET) is the most common neurological movement disorder with few treatments and limited therapeutic efficacy, research into noninvasive and effective treatments is critical. Abnormal cerebello-thalamo-cortical (CTC) loop function are thought to be significant pathogenic causes of ET, with the cerebellum and cortex are common targets for ET treatment. In recent years, transcranial magnetic stimulation (TMS) has been recognized as a promising brain research technique owing to its noninvasive nature and safety. In this study, we will use left M1 cortex continuous theta-burst stimulation (cTBS) combined with right cerebellar hemisphere 1 Hz repetitive transcranial magnetic stimulation (rTMS) dual-target stimulation to explore the Safety, feasibility and efficiency of this dual-target stimulation mode, and the mechanism of its therapeutic effect.

METHODS

Twenty-four patients with ET will be randomly assigned to three groups: dual-target stimulation, single-target stimulation, or sham stimulation. The single-target stimulation group will receive stimulation of the right cerebellar hemisphere for 10 days, whereas the dual-target stimulation group will be given stimulation of both the left M1 cortex and the right cerebellar hemisphere. The sham stimulation group will be given sham stimulation for 10 days. Tremor will be assessed using both the subjective The Essential Tremor Rating Assessment Scale (TETRAS) and objective accelerometer-based tremor analysis. at baseline (before stimulation), after the first, fifth, tenth days of treatment (D1, 5, 10), 24 h after 10 days of treatment (D10-24 h), and 1, 2, 3, and 4 weeks after stimulation (W1, 2, 3, 4).

DISCUSSION

This is a Phase 2 randomized, controlled, patient-assessor blinded clinical trial. The goal of this study is to investigate the Safety, feasibility and efficiency of TMS for the treatment of ET.

摘要

背景

特发性震颤(ET)是最常见的神经运动障碍,治疗方法少且疗效有限,因此研究无创且有效的治疗方法至关重要。小脑 - 丘脑 - 皮质(CTC)环路功能异常被认为是ET的重要致病原因,小脑和皮质是ET治疗的常见靶点。近年来,经颅磁刺激(TMS)因其无创性和安全性,已被公认为一种有前景的脑研究技术。在本研究中,我们将采用左侧M1皮质连续θ波爆发刺激(cTBS)联合右侧小脑半球1Hz重复经颅磁刺激(rTMS)双靶点刺激,以探索这种双靶点刺激模式的安全性、可行性和有效性及其治疗作用机制。

方法

24例ET患者将被随机分为三组:双靶点刺激组、单靶点刺激组或假刺激组。单靶点刺激组将接受右侧小脑半球刺激10天,而双靶点刺激组将同时接受左侧M1皮质和右侧小脑半球刺激。假刺激组将接受10天的假刺激。使用主观的特发性震颤评定量表(TETRAS)和基于加速度计的客观震颤分析来评估震颤。在基线(刺激前)、治疗第1天、第5天、第10天(D1、5、10)、治疗10天后24小时(D10 - 24h)以及刺激后1、2、3和4周(W1、2、3、4)进行评估。

讨论

这是一项2期随机、对照、患者和评估者双盲的临床试验。本研究的目的是调查TMS治疗ET的安全性、可行性和有效性。

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