ChiCTR2200056839 版本V1.4 版本创建时间2022/10/12 20:28:11 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:

ChiCTR2200056839 

最近更新日期:

Date of Last Refreshed on:

2022-10-12 20:25:50 

注册时间:

Date of Registration:

2022-02-19 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

气滞证辨证标准的系统研究—慢性非萎缩性胃炎的临床观察方案

Public title:

Systematic study on syndrome differentiation criteria of Qi stagnation syndrome -- clinical observation scheme of chronic non-atrophic gastritis

注册题目简写:

English Acronym:

研究课题的正式科学名称:

慢性非萎缩性胃炎气滞证证候演变规律及气滞证量表诊断效能的临床研究方案

Scientific title:

Clinical study on the evolution of Qi stagnation syndrome in chronic non-atrophic gastritis and the diagnostic efficacy of Qi stagnation syndrome scale

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:

周旋 

研究负责人:

陈家旭 

Applicant:

Zhou Xuan 

Study leader:

Chen Jiaxu 

申请注册联系人电话:

Applicant telephone:

+86 20 85221323

研究负责人电话:

Study leader's
telephone:

+86 20 85221323

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:

xuetcm@gmail.com

研究负责人电子邮件:

Study leader's E-mail:

chenjiaxu@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:

广东省广州市天河区黄埔大道西601号

研究负责人通讯地址:

广东省广州市天河区黄埔大道西601号

Applicant address:

601 Huangpu Avenue West, Tianhe District, Guangzhou, Guangdong

Study leader's address:

601 Huangpu Avenue West, Tianhe District, Guangzhou, Guangdong

申请注册联系人邮政编码:

Applicant postcode:

510632

研究负责人邮政编码:

Study leader's postcode:

510632

申请人所在单位:

暨南大学中医学院

Applicant's institution:

School of Traditional Chinese Medicine, Ji'nan 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:

JNUKE-2021-046

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:

暨南大学医学伦理委员会

Name of the ethic committee:

Medical Ethics Committee of Ji'nan University

伦理委员会批准日期:

Date of approved by ethic committee:

2021-12-13 00:00:00

伦理委员会联系人:

李老师

Contact Name of the ethic committee:

Ms. Li

伦理委员会联系地址:

广东省广州市天河区黄埔大道西613号

Contact Address of the ethic committee:

613 Huangpu Avenue West, Tianhe District, Guangzhou, Guangdong

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:

暨南大学中医学院

Primary sponsor:

School of Traditional Chinese Medicine, Ji'nan University

研究实施负责(组长)单位地址:

广东省广州市天河区黄埔大道西601号

Primary sponsor's address:

601 Huangpu Avenue West, Tianhe District, Guangzhou, Guangdong

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

广东

市(区县):

广州

Country:

China

Province:

Guangdong

City:

Guangzhou

单位(医院):

暨南大学

具体地址:

天河区黄埔大道西601号

Institution
hospital:

Ji'nan University

Address:

601 Huangpu Avenue West, Tianhe District

经费或物资来源:

广东省科技厅

Source(s) of funding:

Guangdong Provincial Department of Science and Technology

研究疾病:

慢性非萎缩性胃炎  

Target disease:

Chronic Non-Atrophic Gastritis

研究疾病代码:

Target disease code:

研究类型:

观察性研究

Study type:

Observational study

研究所处阶段:

其它 

Study phase:

N/A

研究设计:

横断面 

Study design:

Cross-sectional 

研究目的:

探索气滞证的临床表征及虚实转化规律,评估气滞证诊断量表的诊断效能。  

Objectives of Study:

To explore the clinical characteristics of Qi stagnation syndrome and the law of virtual-real transformation, and to evaluate the diagnostic efficacy of Qi stagnation syndrome diagnostic scale.

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.符合西医诊断标准中慢性非萎缩性胃炎标准;
2.符合中医诊断标准中胃肠气滞证诊断标准;
3.年龄18-65岁之间,性别不限;
4.生命体征平稳,神志清楚,具有一定表达能力;
5.自愿签署知情同意书。

Inclusion criteria

1. Meeting the diagnostic criteria of chronic non-atrophic gastritis in Western medicine;
2. Meet the diagnostic criteria of gastrointestinal Qi stagnation syndrome in the diagnostic criteria of traditional Chinese medicine;
3. Aged between 18 and 65, no gender limit;
4. Stable vital signs, clear consciousness, with certain expression ability;
5. Voluntarily sign the informed consent.

排除标准:

1.合并消化性溃疡,胃镜检查示胃黏膜肠上皮化生、萎缩,上皮内瘤变,病理诊断疑有恶性者;
2.合并有严重糖尿病、心脑血管、肝、肾和造血系统等严重危及生命的原发性疾病者;
3.患有精神病者;
4.妊娠或哺乳期妇女;
5.资料不全等影响观察者。

Exclusion criteria:

1. Patients with peptic ulcer, intestinal metaplasia, atrophy and intraepithelial neoplasia of gastric mucosa by gastroscopy, and suspected malignancy by pathological diagnosis;
2. Patients with severe diabetes, cardiovascular and cerebrovascular diseases, liver, kidney, hematopoietic system and other serious life-threatening primary diseases;
3. Mentally ill;
4. Pregnant or lactating patients;
5. Data not congruent effect observation.

研究实施时间:

Study execute time:

From 2021-12-01 00:00:00 To 2023-09-30 00:00:00  

征募观察对象时间:

Recruiting time:

From 2022-02-14 00:00:00 To 2023-11-30 00:00:00

干预措施:

Interventions:

组别:

连续入组

样本量:

500

Group:

case series

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

广东 

市(区县):

广州 

Country:

China

Province:

Guangdong

City:

Guangzhou

单位(医院):

广东省中医院 

单位级别:

三甲 

Institution
hospital:

Guangdong Provincial Hospital of Traditional Chinese Medicine

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

广东 

市(区县):

广州 

Country:

China

Province:

Guangdong

City:

Guangzhou

单位(医院):

暨南大学附属第一医院 

单位级别:

三甲 

Institution
hospital:

The First Affiliated Hospital of Ji'nan University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

人口学信息

指标类型:

主要指标

Outcome:

Demographic information

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

气滞证中医诊断量表评分

指标类型:

主要指标

Outcome:

Score of TCM diagnostic scale for Qi stagnation syndrome

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

气滞证演变规律观察表

指标类型:

主要指标

Outcome:

Observation table of the evolution of Qi stagnation syndrome

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:

唾液

组织:

Sample Name:

Saliva

Tissue:

人体标本去向

使用后保存  

说明

Fate of sample:

Preservation after use  

Note:

标本中文名:

粪便

组织:

Sample Name:

Stool

Tissue:

人体标本去向

使用后保存  

说明

Fate of sample:

Preservation after use  

Note:

标本中文名:

舌苔

组织:

Sample Name:

Tongue coating

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:

Recruiting status:

尚未开始

Not yet 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):

非随机

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

Not Random.

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

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):

通过文章发表的方式共享数据

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

Sharing data by publishing articles

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:

1.数据收集:分别在合格受试者入组当天0时点、入组后第1周、第2周、第4周4个时点,由临床医生或研究员采用临床观察表(CRF表)对患者相应信息进行收集,收集内容主要包括患者四诊信息、中医证候等; 2.病例记录:使用CRF表对所收集信息进行及时准确的填写,试验过程中发生的任何情况均应详细记录在册。 3.数据保存:每个受试者的CRF表均应妥善保存于安全位置,除研究人员与检察人员之外,其他人无权访问。试验记录应保证真实,不得随意涂改。试验结束后,对每个临床受试者进行身份再识别,确认无误后进行封存。

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

1. Data collection: The Case Record Form (CRF) will be used by the clinician or researcher at 4 time points: the day of enrollment, the first week, the second week, and the fourth week after enrollment. Collect the corresponding information of the patient, and the collected content mainly includes the patient's four-diagnosis information, TCM syndromes, etc.; 2. Case records: Use the CRF to fill in the collected information in a timely and accurate manner. Any situation that occurs during the test should be recorded in detail. 3. Data preservation: The CRF of each subject should be properly kept in a safe place, except for researchers and prosecutors, no one else has the right to access it. The test records shall be authentic and shall not be altered at will. After the test, the identity of each clinical subject was re-identified and sealed after confirmation.

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2022-02-19 12:39:38