ChiCTR2100054895 版本V1.5 版本创建时间2022/12/12 01:42:44 中国临床试验注册中心

审核状态:

Project audit state:

通过审核

Successful

注册号:

Registration number:

ChiCTR2100054895 

最近更新日期:

Date of Last Refreshed on:

2022-06-15 16:24:39 

注册时间:

Date of Registration:

2021-12-28 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

胸椎管狭窄手术术中体感诱发电位和运动诱发电位改变的原因分析,及其与预后价值的关联性:一项前瞻性研究

Public title:

Analysis of altering of somatosensory- and motor- evoked potentials during thoracic spinal surgery and its coerrelation with prognosis: a randomized controlled trial

注册题目简写:

English Acronym:

研究课题的正式科学名称:

胸椎管狭窄手术术中体感诱发电位和运动诱发电位改变的原因分析,及其与预后价值的关联性:一项前瞻性研究

Scientific title:

Analysis of altering of somatosensory- and motor- evoked potentials during thoracic spinal surgery and its coerrelation with prognosis: a randomized controlled trial

研究课题代号(代码):

Study subject ID:

在二级注册机构或其它机构的注册号:

The registration number of the Partner Registry or other register:

申请注册联系人:

刘暾 

研究负责人:

刘暾 

Applicant:

Liu Tun 

Study leader:

Liu Tun 

申请注册联系人电话:

Applicant telephone:

+86 15249254721

研究负责人电话:

Study leader's telephone:

+86 15249254721

申请注册联系人传真 :

Applicant Fax:

研究负责人传真:

Study leader's fax:

申请注册联系人电子邮件:

Applicant E-mail:

405546707@qq.com

研究负责人电子邮件:

Study leader's E-mail:

405546707@qq.com

申请单位网址(自愿提供):

Applicant website(voluntary supply):

研究负责人网址(自愿提供):

Study leader's website(voluntary supply):

申请注册联系人通讯地址:

陕西省西安市碑林区友谊东路555号

研究负责人通讯地址:

陕西省西安市碑林区友谊东路555号

Applicant address:

555 Youyi Road East, Beilin District, Xi'an, Shaanxi

Study leader's address:

555 Youyi Road East, Beilin District, Xi'an, Shaanxi

申请注册联系人邮政编码:

Applicant postcode:

710054

研究负责人邮政编码:

Study leader's postcode:

710054

申请人所在单位:

西安交通大学附属红会医院

Applicant's institution:

Honghui Hospital, Xi'an Jiaotong University

研究负责人所在单位:

西安交通大学附属红会医院

Affiliation of the Leader:

Honghui Hospital, Xi'an Jiaotong University

是否获伦理委员会批准:

是/Yes

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

202111007

伦理委员会批件附件:

Approved file of Ethical Committee:

查看附件View

批准本研究的伦理委员会名称:

西安交通大学附属红会医院伦理委员会

Name of the ethic committee:

Biomedical Research Ethics Committee of Xi'an Honghui Hospital, Xi'an Jiaotong University

伦理委员会批准日期:

Date of approved by ethic committee:

2021-11-29 00:00:00

伦理委员会联系人:

许鹏

Contact Name of the ethic committee:

Xu Peng

伦理委员会联系地址:

西安市碑林区友谊东路555号

Contact Address of the ethic committee:

555 Youyi Road East, Beilin District, Xi'an, Shaanxi

伦理委员会联系人电话:

Contact phone of the ethic committee:

伦理委员会联系人邮箱:

Contact email of the ethic committee:

研究实施负责(组长)单位:

西安交通大学附属红会医院

Primary sponsor:

Xi'an Honghui Hospital, Xi'an Jiaotong University

研究实施负责(组长)单位地址:

西安市碑林区友谊东路555号

Primary sponsor's address:

555 Youyi Road East, Beilin District, Xi'an, Shaanxi

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

陕西

市(区县):

西安

Country:

China

Province:

Shaanxi

City:

Xi'an

单位(医院):

西安交通大学附属红会医院

具体地址:

碑林区友谊东路555号

Institution
hospital:

Xi‘an Honghui Hospital, Xi'an Jiaotong University

Address:

555 Youyi Road East, Beilin District

经费或物资来源:

自筹

Source(s) of funding:

Self-funded

Target disease:

Orthopaedic disease

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

治疗新技术临床试验 

Study phase:

New Treatment Measure Clinical Study

研究设计:

队列研究 

Study design:

Cohort study 

研究目的:

比较两组JOA评分,分析振幅改变率与出院时、术后三个月随访期JOA恢复率的相关性。  

Objectives of Study:

To compare the JOA score between the two groups, and analyzing the correlation between IONM amplitude and JOA recovery ratio at discharge, and at 3-month follow-up.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

1. 18-70岁患者,ASA分级I-III级;
2. CT、MRI检查显示:胸椎管病灶压迫表现;
3. 患者表现为明显胸椎管压迫症状:疼痛、肢体麻木等感觉障碍。

Inclusion criteria

1. Patients aged 18-70 years, ASA I-III;
2. Computed tomography (CT) or magnetic resonance image (MRI) studies showed evidence of thoracic spinal compression;
3. Patients presented obvious thoracic spinal stenosis symptoms, such as pain or numbness in limbs.

排除标准:

1. 患者无法提供知情同意书;
2. 患者既往中锋病史或者有神经系统后遗症;
3. 患者既往接受脊柱手术或其他治疗;
4. 患者酗酒或者毒品史;
5. 患者接受唤醒实验。

Exclusion criteria:

1. Patients were unable to provide informed consent;
2. Patients suffered from the stroke with residual neurological disorder;
3. Patients received other spinal surgery or treatment previously;
4. Patients were alcohol or drug abusers;
5. Patients received wake-up test during decompression surgery.

研究实施时间:

Study execute time:

From 2022-01-15 00:00:00 To 2022-10-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2022-01-15 00:00:00 To 2022-09-01 00:00:00  

干预措施:

Interventions:

组别:

A 组

样本量:

95

Group:

Group A

Sample size:

干预措施:

纠正振幅下降

干预措施代码:

Intervention:

Improve amplitude

Intervention code:

组别:

B组

样本量:

145

Group:

Group B

Sample size:

干预措施:

不纠正振幅下降

干预措施代码:

Intervention:

Do not improve amplitude

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

陕西 

市(区县):

西安 

Country:

China 

Province:

Shaanxi 

City:

Xi'an 

单位(医院):

西安交通大学西安市红会医院 

单位级别:

三甲 

Institution
hospital:

Honghui Hospital, Xi'an Jiaotong University.

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

体感诱发电位振幅

指标类型:

主要指标

Outcome:

Amplitude of SSEP (Somatosensory evoked potential)

Type:

Primary indicator

测量时间点:

术中连续测量

测量方法:

脊柱外科专业电生理记录仪

Measure time point of outcome:

Continually record

Measure method:

An electro-neurophysiological monitor system in spine surgery

指标中文名:

运动诱发电位振幅

指标类型:

主要指标

Outcome:

Amplitude of MEP (Motor evoked potential)

Type:

Primary indicator

测量时间点:

T1:切皮;T2:减压即刻;T3:减压后20分钟;T4:缝合肌肉层

测量方法:

脊柱外科专业电生理记录仪

Measure time point of outcome:

T1, at the start of skin incision; T2, immediately after decompression; T3, 20 minutes after decompression; T4, at the start of surgical muscle closure

Measure method:

An electro-neurophysiological monitor system in spine surgery

指标中文名:

JOA评分

指标类型:

主要指标

Outcome:

JOA (Japanese Orthopaedic Association Scores)

Type:

Primary indicator

测量时间点:

术前,术后

测量方法:

体格检查

Measure time point of outcome:

Preoperative, postoperative

Measure method:

Physical examination

指标中文名:

术后神经功能障碍

指标类型:

主要指标

Outcome:

Postoperative neurological deficits

Type:

Primary indicator

测量时间点:

术后

测量方法:

体格检查

Measure time point of outcome:

Postoperative

Measure method:

Physical examination

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

组织:

Sample Name:

None

Tissue:

人体标本去向

其它  

说明

Fate of sample:

0thers  

Note:

征募研究对象情况:

Recruiting status:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 70 years

性别:

男女均可

Gender:

Both

随机方法(请说明由何人用什么方法产生随机序列):

随机化由统计软件SPSS 24.0产生(IBM; Armonk, 纽约),一个独立的骨科医师负责将患者编号分发给责任麻醉医师。将患者进行分组。一组专业的神经电生理记录医师负责记录数据

Randomization Procedure (please state who generates the random number sequence and by what method):

Randomization was generated by SPSS v24.0 statistics software (IBM; Armonk, NY). An independent orthopedist was in charge of preparing and allocating the patient's number to corresponding anesthesiologists. A team of neurophysiologists was in charge of recording IONM data.

是否公开试验完成后的统计结果:

Calculated Results after the Study Completed public access:

公开/Public

盲法:

Blinding:

试验完成后的统计结果(上传文件):

Calculated Results after
the Study Completed(upload file):

是否共享原始数据:

IPD sharing

Yes

共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址):

原始数据于试验完成后通过临床研究文章形式发表

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

Original data and result will open to the public by clinical papers after the trial complete

数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC:

采用EXCEL表格记录

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

Original documents are managed and stored by the project manager in the excel document database

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2021-12-28 22:42:04