不同疗程针刺治疗膝骨关节炎远期效应评价的随机对照试验

注册号:

Registration number:

ChiCTR2300073383 

最近更新日期:

Date of Last Refreshed on:

2023-09-01 15:55:28 

注册时间:

Date of Registration:

2023-07-10 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

不同疗程针刺治疗膝骨关节炎远期效应评价的随机对照试验

Public title:

Evaluation of the long-term effects of different acupuncture courses for knee osteoarthritis: a randomized controlled trial

注册题目简写:

English Acronym:

研究课题的正式科学名称:

不同疗程针刺治疗膝骨关节炎远期效应评价的随机对照试验

Scientific title:

Evaluation of the long-term effects of different acupuncture courses for knee osteoarthritis: 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:

余英 

研究负责人:

刘存志 

Applicant:

Ying Yu 

Study leader:

Cun-Zhi Liu 

申请注册联系人电话:

Applicant telephone:

+86 188 1136 6020

研究负责人电话:

Study leader's
telephone:

+86 10 5391 2201

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:

y18811366020@163.com

研究负责人电子邮件:

Study leader's E-mail:

lcz_tg@126.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:

北京市朝阳区北三环东路11号

研究负责人通讯地址:

北京市朝阳区北三环东路11号

Applicant address:

11 North Third Ring Road East, Chaoyang District, Beijing

Study leader's address:

11 North Third Ring Road East, Chaoyang District, Beijing

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:

北京中医药大学

Applicant's institution:

Beijing University of Chinese Medicine

研究负责人所在单位:

北京中医药大学

Affiliation of the Leader:

Beijing University of Chinese Medicine

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:

2023BZYLL0506

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:

北京中医药大学医学伦理委员会

Name of the ethic committee:

Medical Ethics Committee of Beijing University of Chinese Medicine

伦理委员会批准日期:

Date of approved by ethic committee:

2023-05-23 00:00:00

伦理委员会联系人:

李梅

Contact Name of the ethic committee:

Mei Li

伦理委员会联系地址:

北京市朝阳区北三环东路11号

Contact Address of the ethic committee:

11 North Third Ring Road East, Chaoyang District, Beijing

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 10 5391 1431

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:

北京中医药大学

Primary sponsor:

Beijing University of Chinese Medicine

研究实施负责(组长)单位地址:

北京市朝阳区北三环东路11号

Primary sponsor's address:

11 North Third Ring Road East, Chaoyang District, Beijing

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

北京

市(区县):

朝阳区

Country:

China

Province:

Beijing

City:

Chaoyang District

单位(医院):

北京中医药大学

具体地址:

北三环东路11号

Institution
hospital:

Beijing University of Chinese Medicine

Address:

11 North Third Ring Road East

经费或物资来源:

刘存志高层次人才科研启动经费

Source(s) of funding:

Liu Cunzhi High-level Talent Research Start-up Grant

研究疾病:

膝骨关节炎  

Target disease:

knee osteoarthritis (KOA)

研究疾病代码:

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:

评估4周对比8周针刺治疗KOA远期效应的差异  

Objectives of Study:

To assess the difference in long-term effect of 4 weeks versus 8 weeks of acupuncture for knee osteoarthritis.

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.有膝关节手术史或正在等待膝关节手术(膝关节置换或膝关节镜手术); 2.其他疾病引起的膝部疼痛(如关节游离体、关节腔严重积液、感染、恶性肿瘤、自身免疫疾病、外伤、骨折、痛风、腰骶椎疾病等); 3.评价关节1年之内有关节镜检查史、近6个月有关节腔注射史; 4.近6月内接受针灸治疗; 5.严重的急性或慢性器质性或精神神经类疾病; 6.凝血功能障碍疾病(如血友病等); 7.具有心脏起搏器或患有癫痫; 8.备孕、妊娠期及哺乳期妇女; 9.近1个月内参加其他临床研究。

Exclusion criteria:

1. History of knee surgery or waiting for surgery (knee replacement or arthroscopic knee surgery); 2. Knee pain caused by other diseases (autoimmune diseases, infection, malignant tumours, trauma, fracture, joint loose bodies, severe effusion of joint cavity, lumbosacral vertebrae disease, gout, etc.); 3. Arthroscopy within 1 year and intra-articular injection in the past 6 months; 4. Acupuncture treatment during the past 6 months; 5. Serious acute or chronic organ diseases or mental disorders; 6. Blood coagulation disorders; 7. Pregnancy and breastfeeding; 8. Cardiac pacemaker and epilepsy; 9. Participation in another clinical study within 1 month.

研究实施时间:

Study execute time:

From 2023-07-10 00:00:00 To 2024-03-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2023-07-10 00:00:00 To 2024-03-31 00:00:00

干预措施:

Interventions:

组别:

4周组

样本量:

74

Group:

4-week acupuncture group

Sample size:

干预措施:

电针治疗4周,每周治疗3次

干预措施代码:

Intervention:

Electro-acupuncture will be administered 3 times a week for a total of 4 weeks

Intervention code:

组别:

8周组

样本量:

74

Group:

8-week acupuncture group

Sample size:

干预措施:

电针治疗8周,每周治疗3次

干预措施代码:

Intervention:

Electro-acupuncture will be administered 3 times a week for a total of 8 weeks

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

北京 

市(区县):

东城区 

Country:

China

Province:

Beijing

City:

Dongcheng District

单位(医院):

东直门医院 

单位级别:

三甲 

Institution
hospital:

Dongzhimen Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

有效应答率

指标类型:

主要指标

Outcome:

Response rate

Type:

Primary indicator

测量时间点:

第26周

测量方法:

Measure time point of outcome:

week 26

Measure method:

指标中文名:

其他时间点的有效应答率

指标类型:

次要指标

Outcome:

Response rates at weeks 4, 8 and 16

Type:

Secondary indicator

测量时间点:

第4、8和16周

测量方法:

Measure time point of outcome:

weeks 4, 8 and 16

Measure method:

指标中文名:

西安大略麦克马斯特大学骨关节炎指数疼痛亚表

指标类型:

次要指标

Outcome:

The Western Ontario and McMaster Universities (WOMAC) Osteoarthritis Index pain subscale

Type:

Secondary indicator

测量时间点:

第0、4、8、16和26周

测量方法:

Measure time point of outcome:

weeks 0, 4, 8, 16 and 26

Measure method:

指标中文名:

西安大略麦克马斯特大学骨关节炎指数功能亚表

指标类型:

次要指标

Outcome:

WOMAC function subscale

Type:

Secondary indicator

测量时间点:

第0、4、8、16和26周

测量方法:

Measure time point of outcome:

weeks 0, 4, 8, 16 and 26

Measure method:

指标中文名:

西安大略麦克马斯特大学骨关节炎指数僵硬亚表

指标类型:

次要指标

Outcome:

WOAMC stiffness subscale

Type:

Secondary indicator

测量时间点:

第0、4、8、16和26周

测量方法:

Measure time point of outcome:

weeks 0, 4, 8, 16 and 26

Measure method:

指标中文名:

简明健康状况调查表12项

指标类型:

次要指标

Outcome:

The Standard 12-item Short Form Health Survey (SF-12)

Type:

Secondary indicator

测量时间点:

第0、4、8、16和26周

测量方法:

Measure time point of outcome:

weeks 0, 4, 8, 16 and 26

Measure method:

指标中文名:

整体疗效评估

指标类型:

次要指标

Outcome:

Patient global assessment

Type:

Secondary indicator

测量时间点:

第0、4、8、16和26周

测量方法:

Measure time point of outcome:

weeks 0, 4, 8, 16 and 26

Measure method:

指标中文名:

国际骨关节炎研究学会应答率

指标类型:

次要指标

Outcome:

The Osteoarthritis Research Society International (OARSI) response rate

Type:

Secondary indicator

测量时间点:

第4、8、16和26周

测量方法:

Measure time point of outcome:

weeks 4, 8, 16 and 26

Measure method:

指标中文名:

备急用药

指标类型:

次要指标

Outcome:

Rescue medicine

Type:

Secondary indicator

测量时间点:

第4、8、16和26周

测量方法:

Measure time point of outcome:

weeks 4, 8, 16 and 26

Measure method:

指标中文名:

数字评价量表

指标类型:

次要指标

Outcome:

numerical rating scale (NRS)

Type:

Secondary indicator

测量时间点:

第0、4、8、16和26周

测量方法:

Measure time point of outcome:

weeks 0, 4, 8, 16 and 26

Measure method:

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 45 years
最大 Max age 75 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):

采用区组随机法,区组长度不固定,随机序列由一位专业的统计学家用SAS 9.3软件产生。

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

A randomization sequence generated using SAS 9.3 software by a professional statistician utilizing block randomization with variable block sizes.

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:

对结局评估者和统计分析人员设盲,对医师和患者不设盲。

Blinding:

The outcome assessor and data analyst will be blinded to group assignments, the acupuncturist and patients will not be blinded.

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

是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):

试验完成后6个月内,通过中国临床试验注册中心的ResMan平台进行原始数据的共享(http://www.medresman.org.cn.)

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

Raw data were shared through the ResMan platform of the China Clinical Trial Registry within 6 months after completion of the trial (http://www.medresman.org.cn.).

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:

通过纸质CRF表格记录元数据,再由两人交叉核对将数据转录到epidata建立的数据库。数据管理由专人负责。

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

The records of metadata are recorded through a CRF form, and then cross-checked and transcribed to an electronic database file based on Epidata software. All the data management is handled by an independent person.

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2023-07-10 09:48:18