针刺太冲配伍太溪穴治疗高血压患者fcMRI脑功能成像研究

注册号:

Registration number:

ChiCTR-TRC-12002427 

最近更新日期:

Date of Last Refreshed on:

2015-09-04 19:58:48 

注册时间:

Date of Registration:

2012-04-08 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

针刺太冲配伍太溪穴治疗高血压患者fcMRI脑功能成像研究

Public title:

An fcMRI Cerebral Functional Imaging Study on Needling in Taichong (LR3) Combining with Taixi (KI3) of hypertension patients

注册题目简写:

English Acronym:

研究课题的正式科学名称:

针刺太冲配伍太溪穴治疗高血压患者fcMRI脑功能成像研究

Scientific title:

An fcMRI Cerebral Functional Imaging Study on Needling in Taichong (LR3) Combining with Taixi (KI3) of hypertension patients

研究课题代号(代码):

Study subject ID:

2012CB518504

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:

黄泳 

研究负责人:

黄泳 

Applicant:

Huang Yong 

Study leader:

Huang Yong 

申请注册联系人电话:

Applicant telephone:

+86 13719189644

研究负责人电话:

Study leader's
telephone:

+86 13719189644

申请注册联系人传真 :

Applicant Fax:

+86 020 61648245

研究负责人传真:

Study leader's fax:

+86 020 61648245

申请注册联系人电子邮件:

Applicant E-mail:

nfhy@fimmu.com

研究负责人电子邮件:

Study leader's E-mail:

nfhy@fimmu.com

申请单位网址(自愿提供):

Applicant website(voluntary supply):

www.fimmu.com

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:

广东省广州市沙太南路1023号南方医科大学中医药学院

研究负责人通讯地址:

广东省广州市沙太南路1023号南方医科大学中医药学院

Applicant address:

1023 South Shatai Road, Guangzhou, Canton, China

Study leader's address:

1023 South Shatai Road, Guangzhou, Canton, China

申请注册联系人邮政编码:

Applicant postcode:

510515

研究负责人邮政编码:

Study leader's postcode:

510515

申请人所在单位:

南方医科大学

Applicant's institution:

Southern Medical University

研究负责人所在单位:

Affiliation of the Leader:

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:

ChiECRCT-2012011

伦理委员会批件附件:

Approved file of Ethical Committee:

批准本研究的伦理委员会名称:

中国注册临床试验伦理审查委员会

Name of the ethic committee:

Chinese clinical trial ethical review committee

伦理委员会批准日期:

Date of approved by ethic committee:

2012-08-01 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:

南方医科大学

Primary sponsor:

Southern Medical University

研究实施负责(组长)单位地址:

广东省广州市沙太南路1023号

Primary sponsor's address:

1023 South Shatai Road, Guangzhou, Canton, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

经费或物资来源:

“973计划”课题基金

Source(s) of funding:

Research Fund of the National Basic Research Program of China (973 Program)

研究疾病:

原发性高血压  

Target disease:

primary hypertension

研究疾病代码:

R544.1

Target disease code:

R544.1

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:

运用fcMRI观察针刺表里经原络配穴后脑功能活动的变化,寻找与经穴循经配伍特异性相关的特异脑区,探讨表里经原络配穴对经穴效应特异性的影响特点及中枢整合机制。 本研究在生理、病理状态下,通过静息态磁共振脑功能成像分析,分别观察针刺太冲穴、太溪穴、非穴和太冲配伍太溪穴、太冲配伍对不同脑区激活效应的变化及其连接,探索针刺治疗高血压的机理,为临床治疗高血压的针刺取穴作理论支持。  

Objectives of Study:

To observe the cerebral functional modification's connections and changes with fcMRI in physical and pathologic conditions when needling Taichong(LR3), Taixi(KI3), non-acupoint, Taichong combining with Taixi, Taichong combining with non-acupoint acupoints, in order to explore the mechanisation of acupunture on the treatment of hypertension and provide theory support for acupuncture treatment of hypertension in the clinical.

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:

健康志愿者排除标准
①近期内(1个月内)患各类疼痛(包括痛经)及失眠等影响治疗效果者;②体内无金属类物质如心脏支架或金属假牙等; ③ 受试穴位处有皮肤病及皮肤破损者; ④患有血小板减少、血友病、凝血功能障碍等疾病;有晕针史者;⑤试验1个月前, 针刺应答预试验无针刺反应者和针刺反应过度敏感者;试验近1个月接受过针刺治疗者;⑥对噪音、低温环境反应强烈及空间幽闭恐惧症患者。
高血压患者排除标准:
①继发性高血压病,妊娠高血压病患者;②合并其他脏器的严重疾病,及糖尿病、血友病、凝血功能障碍等非针刺适应症患者;③精神病患者,孕妇、哺乳期妇女;④受试穴位处有皮肤病及皮肤破损者;⑤在试验观察期间接受其它高血压相关治疗;⑥近期内(1个月内)患各类疼痛(包括痛经)及失眠等影响治疗效果者;⑦有晕针史者;⑧对噪音、低温环境反应强烈及空间幽闭恐惧症患者。

Exclusion criteria:

Healthy volunteers should be excluded:
1. with all kinds of pain (including dysmenorrhea) and insomnia that may affect the treatment effect in the near future (1 month);
2. history of any metallic implant in the body,like heart stent or metal dentures;
3. dermatosis or skin damage near the acupoint where acupuncture would be applied;
4. with thrombocytopenia, hemophilia, blood coagulation dysfunction disease or the history of faintng during acupuncture treatment;
5. no response or excessive sensitive reaction in the acupuncture response pretest which is hold 1 month before the test; received other acupuncture treatment 1 month before the test;
6. Over reactive to noise, low temperature environment and history of claustrophobia.
Hypertension volunteers should be excluded:
1. secondary hypertension, hypertension of pregnancy;
2. With serious disease of other organs, and other diseases like diabetes, hemophilia, coagulant function obstacle patients;
3. Mental patients, pregnancy and nursing mothers;
4. Dermatosis or skin damage near the acupoint where acupuncture would be applied;
5. Received other treatments for hypertension during the experimental observation period;
6. with all kinds of pain (including dysmenorrhea) and insomnia that may affect the treatment effect in the near future (1 month);
7. history of faintng during acupuncture treatment;
8. Over reactive to noise, low temperature environment and history of claustrophobia.

研究实施时间:

Study execute time:

From 2012-06-01 00:00:00 To 2016-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2012-06-01 00:00:00 To 2016-06-30 00:00:00

干预措施:

Interventions:

组别:

太冲高血压患者组

样本量:

12

Group:

P1

Sample size:

干预措施:

针刺太冲穴30分钟,并进行血压测量和fcMRI脑功能成像

干预措施代码:

Intervention:

All subjects reveive acupuncture at Taichong for 30 min, proceed blood pressure measurement and cerebral function imaging by fcMRI

Intervention code:

组别:

太溪高血压患者组

样本量:

12

Group:

P2

Sample size:

干预措施:

针刺太溪穴30分钟,并进行血压测量和fcMRI脑功能成像

干预措施代码:

Intervention:

All subjects reveive acupuncture at Taixi for 30 min, proceed blood pressure measurement and cerebral function imaging by fcMRI

Intervention code:

组别:

太冲穴配伍太溪穴高血压患者组

样本量:

12

Group:

P3

Sample size:

干预措施:

针刺太冲穴配伍太溪穴30分钟,并进行血压测量和fcMRI脑功能成像

干预措施代码:

Intervention:

All subjects reveive acupuncture at Taichong and Taixi acupoints for 30 min, proceed blood pressure measurement and cerebral function imaging by fcMRI

Intervention code:

组别:

非穴高血压患者组

样本量:

12

Group:

P4

Sample size:

干预措施:

针刺非穴30分钟,并进行血压测量和fcMRI脑功能成像

干预措施代码:

Intervention:

All subjects reveive acupuncture at non-acupoint for 30 min, proceed blood pressure measurement and cerebral function imaging by fcMRI

Intervention code:

组别:

太冲配伍非穴高血压患者组

样本量:

12

Group:

P5

Sample size:

干预措施:

针刺太冲配伍非穴30分钟,并进行血压测量和fcMRI脑功能成像

干预措施代码:

Intervention:

All subjects reveive acupuncture at Taichong and non-acupoint for 30 min, proceed blood pressure measurement and cerebral function imaging by fcMRI

Intervention code:

组别:

太冲正常人组

样本量:

12

Group:

N1

Sample size:

干预措施:

针刺太冲穴30分钟,并进行血压测量和fcMRI脑功能成像

干预措施代码:

Intervention:

All subjects reveive acupuncture at Taixi for 30 min, proceed blood pressure measurement and cerebral function imaging by fcMRI

Intervention code:

组别:

太溪正常组

样本量:

12

Group:

N2

Sample size:

干预措施:

针刺太溪穴30分钟,并进行血压测量和fcMRI脑功能成像

干预措施代码:

Intervention:

All subjects reveive acupuncture at Taixi for 30 min, proceed blood pressure measurement and cerebral function imaging by fcMRI

Intervention code:

组别:

太冲穴配伍太溪穴正常人组

样本量:

12

Group:

N3

Sample size:

干预措施:

针刺太冲穴配伍太溪穴30分钟,并进行血压测量和fcMRI脑功能成像

干预措施代码:

Intervention:

All subjects reveive acupuncture at Taichong and Taixi acupoints for 30 min, proceed blood pressure measurement and cerebral function imaging by fcMRI

Intervention code:

组别:

非穴正常人组

样本量:

12

Group:

N4

Sample size:

干预措施:

针刺非穴30分钟,并进行血压测量和fcMRI脑功能成像

干预措施代码:

Intervention:

All subjects reveive acupuncture at non-acupoint for 30 min, proceed blood pressure measurement and cerebral function imaging by fcMRI

Intervention code:

组别:

太冲配伍非穴正常人组

样本量:

12

Group:

N5

Sample size:

干预措施:

针刺太冲配伍非穴30分钟,并进行血压测量和fcMRI脑功能成像

干预措施代码:

Intervention:

All subjects reveive acupuncture at Taichong and non-acupoint for 30 min, proceed blood pressure measurement and cerebral function imaging by fcMRI

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

测量指标:

Outcomes:

指标中文名:

脑功能成像

指标类型:

主要指标

Outcome:

cerebral functional activity

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血压

指标类型:

主要指标

Outcome:

blood pressure

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

不良事件

指标类型:

副作用指标

Outcome:

adverse event

Type:

Adverse events

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:

征募研究对象情况:

Recruiting status:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 65 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):

采用区组随机的方法。严格按照诊断标准、纳入标准和排除标准筛选病例,确定入组后,按照申请随机编码流程获得随机号码,直到完成总观察例数后结束试验。

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

Use randomized block method. Screen volunteers according to the diagnostic criteria, inclusion crit

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:

采用单盲法,即盲病人,采用单间治疗室,保证患者不清楚各自的取穴和操作方法。 数据统计有第三方完成,分析阶段采用盲法统计分析,实行研究者、操作者、统计着三分离。

Blinding:

The study uses the single blind method, concealed to volunteers. Volunteers will be treated in a single therapeutic room ,in oder to ensure that volunteers do not know the others' prescription and treatment methods.

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

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):

南方医科大学

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

Southern Medical University

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:

南方医科大学

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

Southern Medical University

数据与安全监察委员会:

Data and Safety Monitoring Committee:

注册人:

Name of Registration:

 2012-08-18 00:00:00