ChiCTR2300078421 版本V1.0 版本创建时间2023/12/07 16:23:29 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:

ChiCTR2300078421 

最近更新日期:

Date of Last Refreshed on:

2023-12-07 16:22:56 

注册时间:

Date of Registration:

2023-12-07 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

胃充盈超声检查对胃癌的检出及诊断能力研究

Public title:

Study on the ability of gastric filling ultrasonography to detect and diagnose gastric cancer

注册题目简写:

English Acronym:

研究课题的正式科学名称:

胃充盈超声检查对胃癌的检出及诊断能力研究

Scientific title:

Study on the ability of gastric filling ultrasonography to detect and diagnose gastric cancer

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:

刘宇慧 

研究负责人:

严昆 

Applicant:

YuhuiLiu 

Study leader:

Kun Yan 

申请注册联系人电话:

Applicant telephone:

+86 133 7163 1030

研究负责人电话:

Study leader's telephone:

+86 136 1117 6073

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:

wmuliuyuhui@126.com

研究负责人电子邮件:

Study leader's E-mail:

ydbz@vip.sina.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:

阜成路52号, 北京大学肿瘤医院

研究负责人通讯地址:

阜成路52号, 北京大学肿瘤医院

Applicant address:

Peking University Cancer Hospital and Institute, 52 Fucheng Road, Haidian District, Beijing 100142, China

Study leader's address:

Peking University Cancer Hospital and Institute, 52 Fucheng Road, Haidian District, Beijing 100142, China

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:

北京大学肿瘤医院

Applicant's institution:

Peking University Cancer Hospital

研究负责人所在单位:

北京大学肿瘤医院

Affiliation of the Leader:

Peking University Cancer Hospital

是否获伦理委员会批准:

是/Yes

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

2023YJZ50

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:

北京肿瘤医院医学伦理委员会

Name of the ethic committee:

Beijing Cancer Hospital Medical Ethics Committee

伦理委员会批准日期:

Date of approved by ethic committee:

2023-11-20 00:00:00

伦理委员会联系人:

李洁

Contact Name of the ethic committee:

Jie Li

伦理委员会联系地址:

北京市海淀区阜成路81号

Contact Address of the ethic committee:

No.81 Fu-Cheng Road, Haidian District, Beijing

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 10 8819 6391

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:

北京大学肿瘤医院

Primary sponsor:

Peking University Cancer Hospital and Institute

研究实施负责(组长)单位地址:

阜成路52号,海淀区

Primary sponsor's address:

52 Fucheng Road, Haidian District

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):

Country:

CHina

Province:

Beijing

City:

单位(医院):

北京大学肿瘤医院

具体地址:

阜成路52号,海淀区

Institution
hospital:

Peking University Cancer Hospital and Institute

Address:

52 Fucheng Road, Haidian District

经费或物资来源:

北京大学肿瘤医院超声科

Source(s) of funding:

Ultrasound department, Peking University Cancer Hospital and Institute

Target disease:

gastric cancer

Target disease code:

研究类型:

诊断试验

Study type:

Diagnostic test

研究所处阶段:

上市后药物 

Study phase:

4

研究设计:

连续入组 

Study design:

Sequential 

研究目的:

(1)明确胃充盈超声检查对胃癌病灶的检出率 (2)确定胃充盈超声检查提高胃癌术前T分期准确性的可行性  

Objectives of Study:

(1) To determine the detection rate of gastric filling ultrasound for gastric cancer lesions (2) To determine the feasibility of gastric filling ultrasound to improve the accuracy of preoperative T staging of gastric cancer

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) 临床及影像检查确诊的胃癌患者; 2) 拟行手术治疗 3) 患者1月之内未接受药物或放射治疗; 4) 年龄大于18岁; 5) 获得知情同意书的签署。

Inclusion criteria

1) Patients with gastric cancer confirmed by clinical and imaging examination; 2) Surgical treatment is proposed 3) The patient has not received drug or radiation therapy within 1 month; 4) Over 18 years of age; 5) Get the informed consent signed.

排除标准:

1) 豆类蛋白过敏者; 2) 存在胃潴留或急性消化道出血或梗阻等症状,需要禁食或胃肠减压者; 3) 合并重要脏器疾病:如心、肺、肾功能不全; 4) 严重过敏体质; 5) 存在穿刺和手术禁忌症无法获得病理;或患者依从性较差,预计病变无法获得明确诊断; 6) 尚无孕妇使用胃窗造影剂的临床数据,作为预防措施,孕妇及哺乳期女性应避免使用本品。

Exclusion criteria:

1) Soy protein allergy; 2) Gastric retention or acute gastrointestinal bleeding or obstruction, requiring fasting or gastrointestinal decompression; 3) Combined with important organ diseases: such as heart, lung, renal insufficiency; 4) Severe allergies; 5) There are contraindications for puncture and surgery and no pathology can be obtained; Or the patient's compliance is poor, and the lesion is expected to be unable to obtain a clear diagnosis; 6) There is no clinical data on the use of gastric window contrast media in pregnant women. As a precautionary measure, pregnant and lactating women should avoid using this product.

研究实施时间:

Study execute time:

From 2023-11-20 00:00:00 To 2024-11-20 00:00:00  

征募观察对象时间:

Recruiting time:

From 2023-12-10 00:00:00 To 2024-11-20 00:00:00  

诊断试验:

Diagnostic Tests:

金标准或参考标准(即可准确诊断某疾病的单项方法或多项联合方法,在本研究中用于诊断是否有该病的临床参考标准):

手术病理

Gold Standard or Reference Standard (The clinical reference standards required to establish the presence or absence of the target condition in the tested population in present study):

Surgical pathology

指标试验(即本研究的待评估诊断试验,无论为方法、生物标志物或设备,均请列出名称):

胃充盈超声检查

Index test:

gastric filling ultrasonography

目标人群(可以是某种疾病患者或正常人群,详细描述其疾病特征,注意应纳入符合分布特点的全序列病例,具有良好的代表性)

胃癌患者

例数:

Sample size:

280

Target condition (The target condition is a particular disease or disease stage that the index test will be intended to identify. Please specify the characteristics in detail; the population should has a complete spectrum and good representative):

gastric cancer

容易混淆的疾病人群(即与目标疾病不易区分的一种或多种不同疾病,应避免采用正常人群对照的病例-对照设计):

不同分期的胃癌

例数:

Sample size:

280

Population with condition difficult to distinguish from the target condition, the normal population in a case-control study design should be avoid:

different stage of gastric cancer

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):

 

Country:

CHina 

Province:

Beijing 

City:

 

单位(医院):

北京大学肿瘤医院 

单位级别:

三甲 

Institution
hospital:

Peking University Cancer Hospital and Institute

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

T分期准确率

指标类型:

主要指标

Outcome:

T staging accuracy

Type:

Primary indicator

测量时间点:

测量方法:

患者服用造影剂后,对目标病灶进行存图,由两名高年资医师独立分析并汇总结果,不一致的由第三名高年资医师判断讨论,以此得出患者T分期,并与手术病理对照

Measure time point of outcome:

Measure method:

After taking contrast agents, the target lesion was imaged and analyzed independently by two senior physicians who summarized the results. In case of inconsistency, the third senior physician made a judgment and discussion to determine the patient's T-stage, which was compared with surgical pathology

指标中文名:

检出率

指标类型:

主要指标

Outcome:

detection rate

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:

组织:

Sample Name:

None

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction 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 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):

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

None

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

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):

不公开

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

No

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:

检查者填写CRF表并录入excel表格

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

The inspector fills in the CRF form and records the excel form

数据与安全监察委员会:

Data and Safety Monitoring Committee:

暂未确定/Not yet

注册人:

Name of Registration:

 2023-12-07 16:22:56