ChiCTR-IOR-17012847 版本V1.0 版本创建时间2017/10/03 12:23:35 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:

ChiCTR-IOR-17012847 

最近更新日期:

Date of Last Refreshed on:

2017-09-30 11:15:18 

注册时间:

Date of Registration:

2017-09-30 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

电针“骶四穴”与常规电针治疗脑卒中后尿失禁的随机对照临床研究

Public title:

A RCT of electroacupuncture at

注册题目简写:

English Acronym:

研究课题的正式科学名称:

电针“骶四穴”与常规电针治疗脑卒中后尿失禁的随机对照临床研究

Scientific title:

A RCT of electroacupuncture at

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:

陈姗 

研究负责人:

陈姗 

Applicant:

Shan Chen 

Study leader:

Shan Chen 

申请注册联系人电话:

Applicant telephone:

+86 15258813929

研究负责人电话:

Study leader's telephone:

+86 15258813929

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:

breezehilly@hotmail.com

研究负责人电子邮件:

Study leader's E-mail:

breezehilly@hotmail.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:

浙江杭州下沙经济技术开发区9号大街9号

研究负责人通讯地址:

浙江杭州下沙经济技术开发区9号大街9号

Applicant address:

9 Ninth Avenue, Xiasha Economic and Technological Development Zone, Hangzhou, Zhejiang, China

Study leader's address:

9 Ninth Avenue, Xiasha Economic and Technological Development Zone, Hangzhou, Zhejiang, China

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:

浙江中医药大学附属第一医院

Applicant's institution:

The First Affiliated Hospital of Zhejiang Chinese Medical University

研究负责人所在单位:

浙江中医药大学附属第一医院

Affiliation of the Leader:

The First Affiliated Hospital of Zhejiang Chinese Medical 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:

2018-K-059-01

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:

浙江中医药大学附属第一医院伦理委员会

Name of the ethic committee:

Institutional Review Board of The First Affiliated Hospital of Zhejiang Chinese Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2017-07-27 00:00:00

伦理委员会联系人:

Contact Name of the ethic committee:

伦理委员会联系地址:

Contact Address of the ethic committee:

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:

浙江中医药大学附属第一医院

Primary sponsor:

The First Affiliated Hospital of Zhejiang Chinese Medical University

研究实施负责(组长)单位地址:

浙江杭州上城区邮电路54号

Primary sponsor's address:

54 Youdian Road, Shangcheng District, Hangzhou, Zhejiang, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

浙江

市(区县):

Country:

China

Province:

Zhejiang

City:

单位(医院):

浙江中医药大学附属第一医院

具体地址:

浙江杭州上城区邮电路54号

Institution
hospital:

The First Affiliated Hospital of Zhejiang Chinese Medical University

Address:

54 Youdian Road, Shangcheng District, Hangzhou, Zhejiang, China

经费或物资来源:

浙江省中医药管理局

Source(s) of funding:

Zhejiang Provincial Administration of traditional Chinese medicine

Target disease:

Urinary incontinence after stroke

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

其它 

Study phase:

N/A

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

比较电针“骶四穴”和常规电针治疗脑卒中后尿失禁的有效性和安全性  

Objectives of Study:

To compare the efficacy and safety between electroacupuncture at four sacral points and routine electroacupuncture for urinary incontinence after stroke

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)男性或女性,年龄30-85岁;
(2)依据美国中风学会和国际尿控学会诊断为脑卒中后尿失禁的患者;
(3)脑卒中发病后1个月到2年的住院及门诊患者;
(4)生命体征稳定,意识清醒,能够配合治疗;
(5)经药物治疗无效者;
(6)患者或家属知情同意并签署知情同意书。

Inclusion criteria

1. Male or female aged 30-85 years;
2. Patients with UUI after stroke, according to the diagnosis criteria of the American Stroke Association and the ICS
3. Inpatients or outpatients with 4th to 104th week after stroke onset;
4. Stable vital signs, normal consciousness, cooperation with treatment;
5. Refractory to medication;
6. Written informed consent.

排除标准:

(1)同时存在其他疾病导致的尿失禁:帕金森病,多发硬化,脊髓损伤,老年痴呆等;
(2)压力性尿失禁或混合性尿失禁 ;
(3)同时有尿潴留的患者;
(4)有尿道损伤、下尿路梗阻、难治性尿路感染、肾脏积水、泌尿系结石、肿瘤;
(5)严重的认知功能障碍,简易智能状态测试<22分;
(6)患者需大量输液或服用药物影响排尿的;
(7)严重的心、肺、肝、肾等重要脏器功能不全者;
(8)携带植入式电子装置者。

Exclusion criteria:

1. Urinary incontinence caused by other diseases such as Parkinson's disease, multiple sclerosis, spinal injury and Alzheimers disease;
2. Stress urinary incontinence or mixed urinary incontinence
3. Urinary retention in the meantime;
4. Urethral injury, lower urinary tract obstruction, Refractory urinary tract infection, hydronephrosis, urological calculi and tumor;
5. Severe cognitive impairment, MMSE (The Mini-Mental State Examination)<22 points;
6. Large amount of transfusion or medication which influence the function of urination;
7. Insufficiency of heart, lung, live and kidney organs;
8. Wearing implantable electronic device.

研究实施时间:

Study execute time:

From 2017-11-01 00:00:00 To 2020-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2017-10-16 00:00:00 To 2020-10-01 00:00:00  

干预措施:

Interventions:

组别:

电针组

样本量:

60

Group:

eletroacupuncture group

Sample size:

干预措施:

电针“骶四穴”疗法

干预措施代码:

Intervention:

eletroacupuncture at "four sacral points"

Intervention code:

组别:

对照组

样本量:

60

Group:

control group

Sample size:

干预措施:

常规电针疗法

干预措施代码:

Intervention:

routine electroacupuncture

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

浙江 

市(区县):

 

Country:

China 

Province:

Zhejiang 

City:

 

单位(医院):

浙江中医药大学附属第一医院 

单位级别:

三甲医院 

Institution
hospital:

The First Affiliated Hospital of Zhejiang Chinese Medical University

Level of the institution:

Tertiary A hospital

测量指标:

Outcomes:

指标中文名:

漏尿日记

指标类型:

主要指标

Outcome:

Incontinent Episode Diary

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

24 h 尿垫试验

指标类型:

主要指标

Outcome:

24 hour pad test

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

国际尿失禁咨询委员会尿失禁问卷简表

指标类型:

次要指标

Outcome:

International Consultation on Incontinence Questionnaire Urinary Incontinence - Short Form

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

Barthel日常生活能力指数

指标类型:

次要指标

Outcome:

Barthel Activities of Daily Living Index

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:

尿

组织:

Sample Name:

Urine

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

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 30 years
最大 Max age 85 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):

采用SPSS软件由计算机产生随机序列进行分组。

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

The random sequence was generated by using SPSS software in the computer, and the grouping was arranged according to the random sequence.

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

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):

试验完成后6个月内通过Resman共享

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

IPD will be public accessible via ResMan at 2021.6

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:

SPSS数据库

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

SPSS database

数据与安全监察委员会:

Data and Safety Monitoring Committee:

注册人:

Name of Registration:

 2017-09-30 11:15:18