搜风散结方抑制骨侵蚀治疗中晚期类风湿关节炎(痰瘀痹阻证)的临床研究

注册号:

Registration number:

ITMCTR2200006853

最近更新日期:

Date of Last Refreshed on:

2022-12-06

注册时间:

Date of Registration:

2022-12-06

注册号状态:

Registration Status:

预注册

Prospective registration

注册题目:

搜风散结方抑制骨侵蚀治疗中晚期类风湿关节炎(痰瘀痹阻证)的临床研究

Public title:

Clinical study on the treatment of advanced rheumatoid arthritis (Phlegm stasis bi syndrome) by Soufeng Sanjie fomula for inhibiting bone erosion

注册题目简写:

English Acronym:

研究课题的正式科学名称:

医学

Scientific title:

medicine

研究课题的正式科学名称简写:

Scientific title acronym:

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:

ChiCTR2200066446 ; ChiMCTR2200006853

申请注册联系人:

林聃

研究负责人:

胡春萍

Applicant:

lindan

Study leader:

Huchunping

申请注册联系人电话:

Applicant telephone:

18851007068

研究负责人电话:

Study leader's telephone:

13951685111

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:

lin18853856185@163.com

研究负责人电子邮件:

Study leader's E-mail:

njhcp66@126.com

申请单位网址(自愿提供):

Study leader's 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:

江苏省南京市栖霞区江苏省中西医结合医院

研究负责人通讯地址:

江苏省南京市栖霞区江苏省中西医结合医院

Applicant address:

Jiangsu Integrated Traditional Chinese and Western Medicine Hospital, Qixia District, Nanjing city, Jiangsu Province

Study leader's address:

Jiangsu Integrated Traditional Chinese and Western Medicine Hospital, Qixia District, Nanjing city, Jiangsu Province

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:

南京中医药大学附属中西医结合医院

Applicant's institution:

Affiliated Hospital of Integrated Traditional Chinese and Western Medicine of Nanjing University of Chinese Medicine

是否获伦理委员会批准:

Approved by ethic committee:

伦理委员会批件文号:

Approved No. of ethic committee:

2022-LWKY-038

伦理委员会批件附件:

Approved file of Ethical Committee:

查看附件

批准本研究的伦理委员会名称:

江苏省中西医结合医院伦理委员会

Name of the ethic committee:

Ethics Committee of Jiangsu Integrated Traditional Chinese and Western Medicine Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2022/11/29 0:00:00

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:

江苏省中西医结合医院

Primary sponsor:

Jiangsu Integrated Traditional Chinese and Western Medicine Hospital

研究实施负责(组长)单位地址:

江苏省南京市栖霞区江苏省中西医结合医院

Primary sponsor's address:

Jiangsu Integrated Traditional Chinese and Western Medicine Hospital, Qixia District, Nanjing city, Jiangsu Province

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

江苏省

市(区县):

南京市

Country:

China

Province:

Jiangsu

City:

Nanjing

单位(医院):

江苏省中西医结合医院

具体地址:

江苏省南京市栖霞区

Institution
hospital:

Jiangsu Integrated Traditional Chinese and Western Medicine Hospital

Address:

Qixia District, Nanjing City, Jiangsu Province

经费或物资来源:

省级拨款,自筹

Source(s) of funding:

Provincial funding, self-financing

研究疾病:

类风湿关节炎

研究疾病代码:

Target disease:

Rheumatoid arthritis

Target disease code:

研究类型:

Study type:

干预性研究

Interventional study

研究设计:

Study design:

随机平行对照

randomized controlled trial(parallel group design)

研究所处阶段:

Study phase:

探索性研究/预试验

Pilot clinical trial

研究目的:

明确搜风散结方治疗 RA 痰瘀痹阻证患者的疗效及安全性,为以搜风散结方为代表的传统虫药治疗 RA 的药物研发提供科学依据

Objectives of Study:

To clarify the efficacy and safety of Soufeng Sanjie formula in the treatment of patients with PHLEGm-stasis syndrome of RA, and provide scientific basis for the research and development of traditional insecticidal drugs represented by Soufeng Sanjie formula in the treatment of RA

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符合 RA诊断标准及中医痹证(痰瘀痹阻)辨证标准;②年龄18~65岁;③研究开始前3月内未接受慢作用抗风湿药治疗;④研究开始前2周内未接受非甾体抗炎药、激素等药物治疗;⑤自愿签署知情同意书。

Inclusion criteria

① Meet the diagnostic criteria of RA and the syndrome differentiation criteria of TCM bi syndrome (phlegm and blood stasis bi); ② The age ranged from 18 to 65; ③ Did not receive slow-acting anti-rheumatism drugs within 3 months before the study began; ④ No non-steroidal anti-inflammatory drugs, hormones or other drugs were taken within 2 weeks before the study; ⑤ Sign informed consent voluntarily.

排除标准:

①合并肺间质病变;②合并其他结缔组织病;③肝肾功能不全 (AST/ALT、SCr超过正常上限);④未能控制的高血压2级及以上;⑤未能控制的糖尿病,或合并糖尿病靶器官损害;⑥既往消化道溃疡病史;⑦合并严重心脑血管疾病、血液、恶性肿瘤等严重疾病;⑧慢性感染性疾病,包括肝炎、结核等;⑨正在参加其他临床研究的患者;⑩半年内有生育计划的男性患者或有受孕计划的女性患者及妊娠、哺乳期内的患者;怀疑或确有酒精、药物滥用病史,或者根据研究者的判断,具有降低入组可能性或使入组复杂化的其他病变或情况,如工作环境经常变动、生活环境不稳定等易造成失访的情况。

Exclusion criteria:

① Lung interstitial disease; ② With other connective tissue diseases; ③ Liver and kidney dysfunction (AST/ALT and SCr exceeding the normal upper limit); ④ Uncontrolled hypertension grade 2 and above; ⑤ Uncontrolled diabetes, or combined with diabetic target organ damage; ⑥ Previous history of gastrointestinal ulcer; Combined with serious cardiovascular and cerebrovascular diseases, blood, malignant tumors and other serious diseases; ⑧ Chronic infectious diseases, including hepatitis, tuberculosis, etc. ⑨ Patients who are participating in other clinical studies; ⑩ Male patients with fertility plans within six months, female patients with fertility plans, and patients during pregnancy and lactation; Suspected or proven history of alcohol or drug abuse or, in the investigator's judgment, likely to reduce or complicate enrollment

研究实施时间:

Study execute time:

From 2022-12-10

To      2024-04-01

征募观察对象时间:

Recruiting time:

From 2022-12-14

To      2023-03-31

干预措施:

Interventions:

组别:

对照组

样本量:

30

Group:

control group

Sample size:

干预措施:

甲氨蝶呤

干预措施代码:

Intervention:

MTX

Intervention code:

组别:

观察组

样本量:

30

Group:

Observation group

Sample size:

干预措施:

甲氨蝶呤+中药

干预措施代码:

Intervention:

MTX+Traditional Chinese medicine (TCM)

Intervention code:

样本总量 Total sample size : 60

研究实施地点:

Countries of recruitment
and research settings:

国家:

中国

省(直辖市):

江苏省

市(区县):

Country:

China

Province:

Jiangsu

City:

单位(医院):

江苏省中西医结合医院

单位级别:

三甲

Institution/hospital:

Jiangsu Integrated Traditional Chinese and Western Medicine Hospital

Level of the institution:

3 armour

测量指标:

Outcomes:

指标中文名:

肿胀个数

指标类型:

主要指标

Outcome:

Number of swelling

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

关节压痛

指标类型:

主要指标

Outcome:

Joint tenderness

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

中医证候评分

指标类型:

主要指标

Outcome:

TCM syndrome 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:

晨僵时间

指标类型:

主要指标

Outcome:

Morning stiffness time

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

视觉模拟疼痛量表评分(VAS评分)

指标类型:

主要指标

Outcome:

Visual analog pain scale score (VAS 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:

炎症因子

指标类型:

主要指标

Outcome:

Inflammatory cytokines

Type:

Primary 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:

血液

组织:

Sample Name:

Blood

Tissue:

人体标本去向

使用后保存

说明

Fate of sample 

Preservation after use

Note:

征募研究对象情况:

正在进行

Recruiting

年龄范围:

最小 18
Min age years
最大 70
Max age years

Recruiting status:

Participant age:

性别:

Gender:

男女均可

Both

随机方法(请说明由何人用什么方法产生随机序列):

研究负责人采用随机数字表法随机分组

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

Study leaders were randomly assigned using a number table method

盲法:

Blinding:

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):

网络平台-ResMan

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

ResMan

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

数据管理委员会:

Data Managemen Committee:

研究计划书或研究结果报告发表信息
(杂志名称、期、卷、页,时间;或网址):

Publication information of the protocol/research results report
(name of the journal, volume, issue, pages, time; or website):

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