研究疾病:
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脑卒中
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研究疾病代码:
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Target disease:
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stroke
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Target disease code:
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研究类型:
Study type:
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干预性研究
Interventional study
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研究设计:
Study design:
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随机平行对照
randomized controlled trial(parallel group design)
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研究所处阶段:
Study phase:
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其它
Others
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研究目的:
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本项目将通过多中心随机化前瞻性研究,验证早期神经磁调控技术的的风险和疗效;检测推拿技术协同融合的优约性;开发神经移位后神经调控的增强协同作用。通过临床数据、干预数据、检测数据、随访数据的数据集成和分析,提出全病程的多靶区神经调控技术范式;建立促进感觉运动环路重建的增强协同康复临床路径;利用中医推拿技术,开发促进脑卒中运动功能康复的中西医结合创新技术。本项目目标建立基于神经环路调控技术的全病程周期的协同增强康复临床流程,并提高对脑卒中预后和康复的科学评估水平,最终降低脑卒中残疾率。
研究任务一:中枢-外周神经环路磁调控技术在缺血性脑卒中早期的康复疗效研究;
研究任务二:环路神经调控与推拿协同干预在缺血性卒中后中期康复疗效的研究;
研究任务三:神经磁调控在缺血性卒中后神经移位患者中康复疗效研究。
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Objectives of Study:
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This project will verify the risks and efficacy of early neuromagnetic modulation technology through multi-center randomized prospective research; test the superiority of the synergistic fusion of massage technology; develop the enhanced synergy of neuromodulation after neurotranslocation. Through the data integration and analysis of clinical data, intervention data, detection data, and follow-up data, we propose a multi-target neuromodulation technology paradigm throughout the course of the disease; establish an enhanced collaborative rehabilitation clinical path that promotes the reconstruction of sensorimotor circuits; use TCM massage technology to develop Innovative technology combining traditional Chinese and Western medicine to promote the rehabilitation of stroke motor function. The goal of this project is to establish a clinical process of synergy-enhanced rehabilitation based on neural circuit control technology throughout the course of the disease cycle, and improve the level of scientific evaluation of stroke prognosis and rehabilitation, and ultimately reduce the rate of stroke disability.
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药物成份或治疗方案详述:
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1、脑卒中早期神经调控协同增强技术临床试验:首先建立以48小时内康复评估流程,在生命指标稳定的基础上,设计时间窗内的早期综合康复方案,即包括神经调控、运动康复和推拿技术等的临床试验方案。
2、基于神经调控的神经移位技术建立:在神经移位技术的基础上,发展原创性的神经移位-调控融合技术。
3、中西医融合的临床技术研发:基于多靶区神经调控技术,通过多中心前瞻性临床试验研究,重点分析推拿技术在脑卒中的不同阶段(特别在中期阶段)的价值和适宜时间窗。
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Description for medicine or protocol of treatment in detail:
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1. Early stroke neuromodulation synergistic enhancement technology clinical trial: first establish a rehabilitation assessment process within 48 hours, and design an early comprehensive rehabilitation program within a time window on the basis of stable life indicators, including neuromodulation, sports rehabilitation and massage Technology and other clinical trial programs.
2. Establishment of nerve transfer technology based on nerve regulation: On the basis of nerve transfer technology, develop original nerve transfer-regulation fusion technology.
3. Clinical technology research and development of the integration of Chinese and Western medicine: Based on multi-target neuromodulation technology, through multi-center prospective clinical trial research, focus on the analysis of the value and appropriate time window of massage technology in different stages of stroke (especially in the middle stage).
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纳入标准:
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① 临床评估和综合影像学检查确诊为缺血性脑卒中的患者,符合缺血性脑卒中诊断标准;
② Fugl-Meyer运动功能评分证实为运动功能障碍;
③ 年龄18-70周岁,男女不限;
④ 无认知障碍或交流障碍,简易智能状态检查(MMSE)27分以上;
⑤ 首次发病,病程2天-1月。/⑤ 首次发病,病程1月-6月。/⑤ 神经移位术后患者。
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Inclusion criteria
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1. Patients diagnosed as ischemic stroke by clinical evaluation and comprehensive imaging examinations meet the diagnostic criteria for ischemic stroke;
2. Fugl-Meyer motor function score is confirmed as motor dysfunction;
3. Aged 18-70 years, no gender limit;
4. No cognitive impairment or communication impairment, with a score of 27 or more in the Simple Intelligence State Examination (MMSE);
5. The first onset, the course of illness is 2 days to January./ The first onset, the course of illness is from January to June. / Patients after nerve transfer.
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排除标准:
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① 有心肺疾病等严重系统性疾病不能耐受康复治疗者;
② 确诊精神病、重度抑郁症(有自杀倾向)或癫痫患者、有精神病或癫痫的家族史者;
③ 存在糖尿病、尿毒症等严重系统性疾病;
④ 严重的关节挛缩;
⑤ 患有任何原因导致意识障碍;
⑥ 根据安全指南有经颅直流电/磁刺激(TMS/tDCS)和功能磁共振(fMRI)检查的禁忌证如:体内有金属异物或有其它植入体内电子装置等;
⑦ 听觉或视觉上有缺陷可能影响评估及治疗;
⑧ 应用改变大脑皮质兴奋性的药物(抗癫痫药、镇静催眠类药物等)。
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Exclusion criteria:
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1. Those who have serious systemic diseases such as cardiopulmonary disease and cannot tolerate rehabilitation treatment;
2. Patients with diagnosed psychosis, major depression (suicidal tendency) or epilepsy, and those with family history of psychosis or epilepsy;
3. Existence of serious systemic diseases such as diabetes and uremia;
4. Severe joint contracture;
5. Suffer from any cause of consciousness disorder;
6. According to safety guidelines, there are contraindications for transcranial direct current/magnetic stimulation (TMS/tDCS) and functional magnetic resonance (fMRI) examinations such as: metal foreign bodies in the body or other electronic devices implanted in the body;
7. Defects in hearing or vision may affect assessment and treatment;
8. Use drugs that change the excitability of the cerebral cortex (antiepileptic drugs, sedative hypnotic drugs, etc.).
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研究实施时间:
Study execute time:
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从From
2020-09-01
至To
2022-09-01
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征募观察对象时间:
Recruiting time:
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从From
2020-09-01
至To
2022-08-31
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