ChiCTR-TRC-11001408 版本V1.3 版本创建时间2015/07/12 16:05:22 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-TRC-11001408 

最近更新日期:

Date of Last Refreshed on:

2015-07-12 16:03:40 

注册时间:

Date of Registration:

2011-07-01 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

艾灸治疗膝骨关节炎的随机双盲对照临床试验

Public title:

Moxibustion treatment in Osteoarthritis of the Knee: a randomized double-blinding control trial

注册题目简写:

English Acronym:

研究课题的正式科学名称:

艾灸治疗膝骨关节炎的随机双盲对照临床试验

Scientific title:

Moxibustion treatment in Osteoarthritis of the Knee: a randomized double-blinding control 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:

赵玲 

研究负责人:

沈雪勇 

Applicant:

Ling Zhao 

Study leader:

Xueyong Shen 

申请注册联系人电话:

Applicant telephone:

+86 13917674196

研究负责人电话:

Study leader's
telephone:

+86 13361838083

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:

zhao099@hotmail.com

研究负责人电子邮件:

Study leader's E-mail:

snowysh@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:

上海市蔡伦路1200号149信箱

研究负责人通讯地址:

上海市蔡伦路1200号150信箱

Applicant address:

149 box,1200 Cailun Road, Shanghai, China

Study leader's address:

150 box, 1200 Cailun Road, Shanghai, China

申请注册联系人邮政编码:

Applicant postcode:

201203

研究负责人邮政编码:

Study leader's postcode:

201203

申请人所在单位:

上海中医药大学

Applicant's institution:

Shanghai University of Traditional Chinese Medicine

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-20110022

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:

Institutional Ethic Review Committee of Chinese Clinical Trials Registry

伦理委员会批准日期:

Date of approved by ethic committee:

2011-06-28 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:

上海中医药大学

Primary sponsor:

Shanghai University of Traditional Chinese Medicine

研究实施负责(组长)单位地址:

上海市蔡伦路1200号

Primary sponsor's address:

1200 Cailun Road, Shanghai, 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):

上海

市(区县):

Country:

China

Province:

Shanghai

City:

单位(医院):

上海市科委

具体地址:

上海祖冲之路1559

Institution
hospital:

Shanghai Science and Technology Developing Foundation

Address:

1559 Zuchongzhi Road, Shanghai, China

经费或物资来源:

上海市科委

Source(s) of funding:

Shanghai Science and Technology Developing Foundation

研究疾病:

膝骨关节炎  

Target disease:

knee osteoarthritis

研究疾病代码:

M19.966

Target disease code:

M19.966

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

II期临床试验 

Study phase:

2

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

通过一项随机对照临床试验,观察艾灸治疗膝骨关节炎患者的有效性和安全性。  

Objectives of Study:

To conduct a phase II randomized placebo-controlled clinical trial to evaluate the efficacy and safety of moxibustion therapy in patients with knee OA.

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.年龄45~75周岁
2.签署知情同意书
3.符合美国风湿病学院标准诊断膝骨关节炎标准,至少6个月病程
4.在过去一个月中大部分日子里膝关节至少中度疼痛
5.病人可以继续服用参与本试验前所使用的相关药物,如控制疼痛采用镇痛剂或非类固醇抗炎药等,但是不能服用激素类药物,并同意在治疗过程中不随意更换药物者
6.有X线证明骨关节炎的变化(K&L评分>2)

Inclusion criteria

1. Male and female aged 45 to 75 years old;
2. Able and willing to provide signed informed consent;
3. Have a diagnosis of osteoarthritis of the knee (fulfilling ACR criteria) for at least 6 months;
4. have at least moderate pain in the knee for most days of the past month;
5. be taking analgesic or nonsteroidal anti-inflammatory agents (NSAIDs), but not corticosteroids, but will be asked to document use;
6. have documented radiographic osteoarthritis changes (Kellgren-Lawrence grade>2).

排除标准:

1.过去3个月内接受激素治疗者;
2.过去6个月内接受关节内透明质酸酶注射;
3.过去1年内接受了关节冲洗或关节内窥镜检查;
4.妨碍实验设计的安全参与和影响研究完成的疾病,如过去3个月患有心肌梗塞或中风、充血性心力衰竭、严重慢性阻塞性肺疾患、癌症、糖尿病、严重的全身性疾病及严重精神病;
5.过去30天内使用过任何试验药物;
6.有出血倾向体质病史或临床表现,包括目前正在使用抗凝剂
7.炎性关节炎(如类风湿或银屑病型)
8.同时参与其他研究;
9.曾做过膝关节置换手术者;
10.过去接受过艾灸治疗;
11.对艾灸烟雾过敏者;
12.同时局部使用外治疗法,如局部贴敷治疗等;
13.无法完成各种量表填写

Exclusion criteria:

1. corticosteroid treatment within the past 3 months;
2. intra-articular (IA) injection within the past 6 months;
3. joint lavage or joint endoscopy examination within the past year;
4. uncontrolled medical condition,which could affect the trial, such as cancer;
5. use of any investigational drug within the past 30 days;
6. bleeding tendency,including the use of anticoagulants;
7. other arthritis such as rheumatoid arthritis;
8. participating other trials at the same time;
9. former knee joint surgery;
10. prior experience with moxibustion treatment;
11. allergy to moxa smoke;
12. applying local exteranl therapy, e.g. local pasting with chinese medication
13. unable to fulfil the forms.

研究实施时间:

Study execute time:

From 2009-09-01 00:00:00 To 2011-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2009-09-06 00:00:00 To 2011-11-30 00:00:00

干预措施:

Interventions:

组别:

1

样本量:

51

Group:

1

Sample size:

干预措施:

取内、外膝眼、阿是穴,采用治疗艾炷,每穴每次灸3壮,隔日一次,每周3次,连续治疗6周,共18次

干预措施代码:

Intervention:

applying true moxa cone on the points ST35, EX-LE4 and Ashi point around the knees, three moxa cone every point, once a day, three times a week for six weeks, total 18 times.

Intervention code:

组别:

2

样本量:

51

Group:

2

Sample size:

干预措施:

取内、外膝眼、阿是穴,采用安慰艾炷,每穴每次灸3壮安慰艾炷,隔日一次,每周3次,连续治疗6周,共18次

干预措施代码:

Intervention:

applying sham moxa cones on the points ST35, EX-LE4 and Ashi point around the knees, three moxa cone every point,once a day, three times a week for six weeks, total 18 times.

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

上海 

市(区县):

 

Country:

China

Province:

Shanghai

City:

单位(医院):

浦东新区中医院 

单位级别:

浦东新区中医院 

Institution
hospital:

Pudong New District Hospital ofTraditional Chinese Medicine of Shanghai

Level of the institution:

Secondary B hospital

测量指标:

Outcomes:

指标中文名:

西安大略和麦克马斯特大学骨关节炎调查量表(WOMAC)

指标类型:

主要指标

Outcome:

Western Ontario and McMaster Universities' Osteoarthritis Index (WOMAC) score

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

patient global assessment

指标类型:

次要指标

Outcome:

patient global assessment

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

SF-36生存质量调查问卷

指标类型:

次要指标

Outcome:

36-Item Short-Form Health Survey (SF-36)

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血清中COMP,IL-1β和COX-2的含量

指标类型:

附加指标

Outcome:

Serum COMP, IL-1beta and COX-2 levels

Type:

Additional 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:

征募研究对象情况:

Recruiting status:

结束

/Completed

年龄范围:

Participant age:

最小 Min age 16 years
最大 Max age 80 years

性别:

男性

Gender:

Male

随机方法(请说明由何人用什么方法产生随机序列):

随机数字表

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

randomization table

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

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):

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

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:

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

数据与安全监察委员会:

Data and Safety Monitoring Committee:

注册人:

Name of Registration:

 2015-07-12 16:03:40