中国神经再生研究(英文版) ›› 2022, Vol. 17 ›› Issue (11): 2491-2496.doi: 10.4103/1673-5374.339011

• 原著:脑损伤修复保护与再生 • 上一篇    下一篇

不同频率重复经颅磁刺激联合A型肉毒毒素局部注射治疗脑卒中后下肢肌肉痉挛的最佳方案:前瞻性、单中心、非随机、对照临床试验方案

  

  • 出版日期:2022-11-15 发布日期:2022-04-22

Different frequencies of repetitive transcranial magnetic stimulation combined with local injection of botulinum toxin type A for post-stroke lower limb spasticity: study protocol for a prospective, single-center, non-randomized, controlled clinical trial

Yang Shao, Yang Yang, Yong-Xin Sun, Ai-Hua Xu*   

  1. Department of Rehabilitation Medicine, the First Affiliated Hospital of China Medical University, Shenyang, Liaoning Province, China
  • Online:2022-11-15 Published:2022-04-22
  • Contact: Ai-Hua Xu, PHD, ahxu@cmu.edu.cn.

摘要:

目前临床上对于低频或高频重复经颅磁刺激治疗脑卒中后肌肉痉挛的疗效及安全性尚无确切的共识。最新的研究表明,低频重复经颅磁刺激联合A型肉毒毒素局部注射治疗脑卒中后肢体痉挛的效果优于单独应用A型肉毒毒素局部注射。为此,课题组设计了一项前瞻性、单中心、非随机对照临床试验方案,以观察不同频率重复经颅磁刺激联合A型肉毒毒素局部注射治疗脑卒中后下肢肌肉痉挛的疗效及安全性差异,希望能确定一套最佳治疗方案。收集中国医科大学附属第一医院康复医学科的脑卒中后肌肉痉挛患者150例,均进行常规康复训练,并以脑梗死面积和治疗方式不同进行试验分组。A组:大面积脑梗死患者,A型肉毒毒素局部注射+健侧低频重复经颅磁刺激(1 Hz);B组:非大面积脑梗死患者,A型肉毒毒素局部注射+患侧高频重复经颅磁刺激(10-20 Hz);C组:大面积/非大面积脑梗死患者,A型肉毒毒素局部注射;D组:大面积脑梗死患者,健侧低频重复经颅磁刺激(1 Hz);E组:非大面积脑梗死患者,患侧高频重复经颅磁刺激(10-20 Hz),共5组,每组30例。试验主要结局指标为治疗前1 d至治疗后12个月的改良Ashworth痉挛量表评分变化;次要结局指标为治疗前1 d至治疗后12个月的Fugl-Meyer下肢运动功能量表评分、患肢目测类比评分、Berg平衡量表评分、改良Barthel指数量表评分,安全性指标为治疗后3-12个月的不良事件发生率。试验希望观察不同频率重复经颅磁刺激联合A型肉毒毒素局部注射治疗脑卒中下肢肌肉痉挛的疗效及安全性差异,筛选出治疗脑卒中后下肢肌肉痉挛的最佳方案。试验开始时间2021-12-01,实验结束时间2023-12-30。试验方案已经中国医科大学附属第一医院医学科学研究伦理委员会审批,伦理批件号:科伦审[2021]2021-333-3号,批准时间:2021-08-19。试验已经于中国临床试验注册中心注册(注册号:ChiCTR2100052180,注册时间:2021-10-21),方案版本号1.1。

https://orcid.org/0000-0002-2447-3692 (Ai-Hua Xu)

关键词: 重复经颅磁刺激, 脑卒中, A型肉毒毒素, 肌肉痉挛, 下肢, 运动, 康复训练, 神经再生

Abstract: No definite consensus has currently been reached regarding the safety and efficacy of low- or high-frequency repetitive transcranial magnetic stimulation in the treatment of post-stroke muscle spasticity. The latest research indicates that when combined with local injections of botulinum toxin type A, it is more effective on post-stroke muscle spasticity than local injections of botulinum toxin type A alone. We designed a prospective, single-center, non-randomized, controlled clinical trial to investigate the safety and efficacy of different frequencies of repetitive transcranial magnetic stimulation combined with local injections of botulinum toxin type A in treating post-stroke lower limb muscle spasticity to determine an optimal therapeutic regimen. This trial will enroll 150 patients with post-stroke muscle spasticity admitted to the Department of Rehabilitation Medicine at the First Affiliated Hospital of China Medical University. All enrolled patients will undergo routine rehabilitation training and will be divided into five groups (n = 30 per group) according to the particular area of cerebral infarction and treatment methods. Group A: Patients with massive cerebral infarction will be given local injections of botulinum toxin type A and low-frequency (1 Hz) repetitive transcranial magnetic stimulation on the contralateral side; Group B: Patients with non-massive cerebral infarction will be given local injections of botulinum toxin type A and high-frequency (10–20 Hz) repetitive transcranial magnetic stimulation on the affected side; Group C: Patients with massive/non-massive cerebral infarction will be given local injections of botulinum toxin type A; Group D: Patients with massive cerebral infarction will be given low-frequency (1 Hz) repetitive transcranial magnetic stimulation on the contralateral side; and Group E: Patients with non-massive cerebral infarction will be given high-frequency (10–20 Hz) repetitive transcranial magnetic stimulation on the affected side. The primary outcome measure of this trial is a modified Ashworth scale score from 1 day before treatment to 12 months after treatment. Secondary outcome measures include Fugl-Meyer Assessment of Lower Extremity, Visual Analogue Scale, modified Barthel index, and Berg Balance Scale scores for the same time as specified for primary outcome measures. The safety indicator is the incidence of adverse events at 3–12 months after treatment. We hope to draw a definite conclusion on whether there are differences in the safety and efficacy of low- or high-frequency repetitive transcranial magnetic stimulation combined with botulinum toxin type A injections in the treatment of patients with post-stroke lower limb spasticity under strict grouping and standardized operation, thereby screening out the optimal therapeutic regimen. The study protocol was approved by the Medical Ethics Committee of the First Affiliated Hospital of China Medical University (approval No. [2021] 2021-333-3) on August 19, 2021. The trial was registered with the Chinese Clinical Trial Registry (Registration No. ChiCTR2100052180) on October 21, 2021. The protocol version is 1.1.

Key words: Botulinum toxin type A, exercise, lower limbs, muscle spasticity, neural regeneration, rehabilitation training, repetitive transcranial magnetic stimulation, stroke