低场强移动磁共振在脑脊液内引流术后调压中的应用研究

注册号:

Registration number:

ChiCTR2300077352 

最近更新日期:

Date of Last Refreshed on:

2024-05-24 22:12:38 

注册时间:

Date of Registration:

2023-11-06 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

低场强移动磁共振在脑脊液内引流术后调压中的应用研究

Public title:

Application of portable low-field magnetic resonance imaging in postoperative pressure regulation of cerebrospinal fluid drainage

注册题目简写:

English Acronym:

研究课题的正式科学名称:

低场强移动磁共振在脑脊液内引流术后调压中的应用研究

Scientific title:

Application of portable low-field magnetic resonance imaging in postoperative pressure regulation of cerebrospinal fluid drainage

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:

肖青山 

研究负责人:

郭燕舞 

Applicant:

Qingshan Xiao 

Study leader:

Yanwu Guo 

申请注册联系人电话:

Applicant telephone:

+86 198 8083 2529

研究负责人电话:

Study leader's
telephone:

+86 198 8083 2529

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:

764351857@qq.com

研究负责人电子邮件:

Study leader's E-mail:

764351857@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:

广东省广州市海珠区南石头街道工业大道253号

研究负责人通讯地址:

广东省广州市海珠区南石头街道工业大道253号

Applicant address:

253 Industrial Avenue, Nanshitou Street, Haizhu District, Guangzhou, Guangdong

Study leader's address:

253 Industrial Avenue, Nanshitou Street, Haizhu District, Guangzhou, Guangdong

申请注册联系人邮政编码:

Applicant postcode:

研究负责人邮政编码:

Study leader's postcode:

申请人所在单位:

珠江医院

Applicant's institution:

Zhujiang Hospital

研究负责人所在单位:

珠江医院

Affiliation of the Leader:

Zhujiang Hospital

是否获伦理委员会批准:

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

2022-KY-290-02

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:

南方医科大学珠江医院伦理委员会

Name of the ethic committee:

Ethics Committee of Pearl River Hospital of Southern Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2023-05-11 00:00:00

伦理委员会联系人:

黄熙华

Contact Name of the ethic committee:

Huang Xihua

伦理委员会联系地址:

广东省广州市海珠区南石头街道工业大道253号

Contact Address of the ethic committee:

253 Industrial Avenue, Nanshitou Street, Haizhu District, Guangzhou, Guangdong

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 20 6278 3254

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:

珠江医院

Primary sponsor:

Zhujiang Hospital

研究实施负责(组长)单位地址:

广东省广州市海珠区南石头街道工业大道253号

Primary sponsor's address:

253 Industrial Avenue, Nanshitou Street, Haizhu District, Guangzhou, Guangdong

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

广东

市(区县):

Country:

China

Province:

Guangdong

City:

单位(医院):

珠江医院

具体地址:

广东省广州市海珠区南石头街道工业大道253号

Institution
hospital:

Zhujiang Hospital

Address:

253 Industrial Avenue, Nanshitou Street, Haizhu District, Guangzhou, Guangdong

经费或物资来源:

Source(s) of funding:

No

研究疾病:

脑积水  

Target disease:

Hydrocephalus

研究疾病代码:

Target disease code:

研究类型:

观察性研究

Study type:

Observational study

研究所处阶段:

探索性研究/预试验 

Study phase:

0

研究设计:

队列研究 

Study design:

Cohort study 

研究目的:

观察可调压分流管调压阀门在低场强移动磁共振下的稳定性,研究脑积水分流术后患者行低场强磁共振检查的安全性。评价低场强移动磁共振在分流术后调压重点应用价值。  

Objectives of Study:

To observe the stability of the adjustable pressure shunt tube pressure regulating valve under low-field mobile magnetic resonance, and to study the safety of low-field magnetic resonance examination in patients after hydrocephalus flow surgery. To evaluate the key application value of low field strength mobile magnetic resonance in postoperative pressure regulation of shunting.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

Inclusion criteria

排除标准:

1.心脏起搏器或除颤器、静脉药物泵、胰岛素泵、深部脑刺激器、迷走神经刺激器、耳蜗等植入者; 2.持续的体外膜氧合治疗和心肺功能不稳定、意识障碍或抽搐、严重头痛呕吐,磁共振检查过程可能出现生命危险者; 3.幽闭恐惧症或其他无法配合磁共振检查的精神、心理障碍者; 4.计划妊娠、意外妊娠以及妊娠者。

Exclusion criteria:

1. Pacemaker or defibrillator, intravenous drug pump, insulin pump, deep brain stimulator, vagus nerve stimulator, cochlear implant, etc.; 2. Continuous extracorporeal membrane oxygenation therapy and cardiopulmonary instability, impaired consciousness or convulsions, severe headache and vomiting, and life-threatening conditions during magnetic resonance examination; 3. Claustrophobia or other mental or psychological disorders that cannot cooperate with magnetic resonance examination; 4. Planned pregnancy, unintended pregnancy, and pregnancy.

研究实施时间:

Study execute time:

From 2022-08-01 00:00:00 To 2023-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2022-09-07 00:00:00 To 2023-09-30 00:00:00

干预措施:

Interventions:

组别:

根据分流管品牌分组

样本量:

40

Group:

Group according to the brand of the diversion pipe

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

广东 

市(区县):

 

Country:

China

Province:

Guangdong

City:

单位(医院):

珠江医院 

单位级别:

三甲 

Institution
hospital:

Zhujiang Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

分流阀压力值

指标类型:

主要指标

Outcome:

Shunt valve pressure value

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

Evans指数

指标类型:

次要指标

Outcome:

Evans index

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

z-Evans指数和脑/脑室比率

指标类型:

次要指标

Outcome:

Z-Evans index and brain/ventricular ratio

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

胼胝体角

指标类型:

次要指标

Outcome:

Callosum horn

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

组织:

Sample Name:

No

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:

结束

/Completed

年龄范围:

Participant age:

最小 Min age 0 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):

不适用

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

N/A

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

否No

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):

临床试验公共管理平台,http://www.medresman.org.cn/login.aspx

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

Clinical Trail Management Public Platform, http://www.medresman.org.cn/login.aspx

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:

ResMan

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

ResMan

数据与安全监察委员会:

Data and Safety Monitoring Committee:

暂未确定/Not yet

注册人:

Name of Registration:

 2023-11-06 16:01:45