胶囊内窥镜AKEM-31SW/AKES-31SW初步临床研究

注册号:

Registration number:

ChiCTR2100042427 

最近更新日期:

Date of Last Refreshed on:

2021-04-24 23:57:54 

注册时间:

Date of Registration:

2021-01-21 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

胶囊内窥镜AKEM-31SW/AKES-31SW初步临床研究

Public title:

Preliminary clinical study of capsule endoscopy AKEM-31SW/AKES-31SW

注册题目简写:

English Acronym:

研究课题的正式科学名称:

胶囊内窥镜AKEM-31SW/AKES-31SW初步临床研究

Scientific title:

Preliminary clinical study of capsule endoscopy AKEM-31SW/AKES-31SW

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:

白涛 

研究负责人:

侯晓华 

Applicant:

Tao Bai 

Study leader:

Xiaohua Hou 

申请注册联系人电话:

Applicant telephone:

+86 15802734363

研究负责人电话:

Study leader's
telephone:

+86 27-85726057

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:

drbaitao@126.com

研究负责人电子邮件:

Study leader's E-mail:

houxh@hust.edu.cn

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:

湖北省武汉市解放大道1277号

研究负责人通讯地址:

湖北省武汉市解放大道1277号

Applicant address:

1277 Jiefang Avenue, Wuhan, Hubei

Study leader's address:

1277 Jiefang Avenue, Wuhan, Hubei

申请注册联系人邮政编码:

Applicant postcode:

430022

研究负责人邮政编码:

Study leader's postcode:

430022

申请人所在单位:

华中科技大学同济医学院附属协和医院

Applicant's institution:

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

研究负责人所在单位:

华中科技大学同济医学院附属协和医院

Affiliation of the Leader:

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

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:

[2020]伦审字(0519)号

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:

华中科技大学同济医学院附属协和医院医学伦理委员会

Name of the ethic committee:

Medical Ethics Committee of Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

伦理委员会批准日期:

Date of approved by ethic committee:

2021-01-12 00:00:00

伦理委员会联系人:

吴建才

Contact Name of the ethic committee:

Jiancai Wu

伦理委员会联系地址:

湖北省武汉市解放大道1277号

Contact Address of the ethic committee:

1277 Jiefang Avenue, Wuhan, Hubei

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:

华中科技大学同济医学院附属协和医院

Primary sponsor:

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

研究实施负责(组长)单位地址:

湖北省武汉市解放大道1277号

Primary sponsor's address:

1277 Jiefang Avenue, Wuhan, Hubei

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

湖北

市(区县):

武汉

Country:

China

Province:

Hubei

City:

Wuhan

单位(医院):

华中科技大学同济医学院附属协和医院

具体地址:

解放大道1277号

Institution
hospital:

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Address:

1277 Jiefang Avenue, Jianghan District

经费或物资来源:

自筹

Source(s) of funding:

Self financing

研究疾病:

胃和/或小肠疾病检查  

Target disease:

Examination of stomach and / or small intestine diseases

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:

探索性研究/预试验 

Study phase:

0

研究设计:

非随机对照试验 

Study design:

Non randomized control 

研究目的:

探讨新型AKEM-31SW/AKES-31SW型胶囊内镜的临床应用可行性及检查效能。  

Objectives of Study:

To investigate the clinical application feasibility and examination efficiency of the new AKEM-31SW/AKES-31SW capsule endoscopy.

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)三个月内参加过其他临床试验或正在参加其他临床试验的患者;
2)无手术条件或拒绝接受任何腹部手术者(一旦胶囊滞留将无法通过手术取出);
3)体内装有心脏起搏器,但除外起搏器为新型MRI兼容性产品的情况;
4)体内植入电子耳蜗、磁性金属药物灌注泵、神经刺激器等电子装置以及磁性金属异物;
5)胶囊内镜排出体外前计划行核磁共振(MRI)检查者;
6)已知或怀疑胃肠道梗阻、狭窄、憩室、瘘管或活动性大出血;
7)既往有影响消化道正常结构的腹部手术史;
8)妊娠期女性;
9)精神疾病患者;
10)严重哮喘、吞咽障碍或胃瘫等排空障碍;
11)一般情况差,不能耐受MCE检查者;
12)研究人员认为存在任何其他不适合受试者参与研究的影响因素。

Exclusion criteria:

1) Patients who have participated in other clinical trials or are participating in other clinical trials within three months;
2) Those who have no surgical conditions or refuse to accept any abdominal surgery (once the capsule is retained, it will not be removed by surgery);
3) Cardiac pacemaker is installed in the body, except that the pacemaker is a new MRI compatible product;
4) Cochlear implant, magnetic metal drug infusion pump, nerve stimulator and other electronic devices and magnetic metal foreign bodies were implanted in vivo;
5) MRI examination was planned before capsule endoscopy was discharged;
6) Gastrointestinal obstruction, stenosis, diverticulum, fistula or active massive hemorrhage are known or suspected;
7) Previous abdominal operation history affecting normal structure of digestive tract;
8) Pregnant women;
9) Patients with mental illness;
10) Severe asthma, dysphagia, gastroparesis and other emptying disorders;
11) The general condition was poor, and could not tolerate MCE examination;
12) The researchers believe that there are any other factors that are not suitable for subjects to participate in the study.

研究实施时间:

Study execute time:

From 2021-02-15 00:00:00 To 2021-09-15 00:00:00  

征募观察对象时间:

Recruiting time:

From 2021-02-15 00:00:00 To 2021-09-15 00:00:00

干预措施:

Interventions:

组别:

AKES-31SW组

样本量:

20

Group:

AKES-31SW group

Sample size:

干预措施:

AKES-31SW胶囊内镜检查

干预措施代码:

Intervention:

AKES-31SW capsule endoscopy check up

Intervention code:

组别:

GIVEN组

样本量:

40

Group:

GIVEN group

Sample size:

干预措施:

GIVEN胶囊检查

干预措施代码:

Intervention:

GIVEN capsule endoscopy check up

Intervention code:

组别:

AKEM-11SW组

样本量:

40

Group:

AKEM-11SW group

Sample size:

干预措施:

AKEM-11SW胶囊检查

干预措施代码:

Intervention:

AKEM-11SW capsule endoscopy check up

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

湖北 

市(区县):

武汉 

Country:

China

Province:

Hubei

City:

Wuhan

单位(医院):

华中科技大学同济医学院附属协和医院 

单位级别:

三级 

Institution
hospital:

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

湖北 

市(区县):

武汉 

Country:

China

Province:

Hubei

City:

Wuhan

单位(医院):

武汉市第六人民医院 

单位级别:

三级 

Institution
hospital:

Wuhan Sixth People's Hospital

Level of the institution:

Tertiary

测量指标:

Outcomes:

指标中文名:

胃肠道各部观察完整性

指标类型:

主要指标

Outcome:

The completeness of GI tract examination

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

不良事件发生率

指标类型:

主要指标

Outcome:

Incidence of adverse events

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

吞咽胶囊舒适度

指标类型:

次要指标

Outcome:

Comfort of swallowing capsule

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

胶囊内镜操控性能

指标类型:

次要指标

Outcome:

Manipulation performance of capsule endoscopy

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

检查相关时间指标

指标类型:

次要指标

Outcome:

Check the relevant time indicators

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

图像质量

指标类型:

次要指标

Outcome:

Image quality

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

病变检出率

指标类型:

次要指标

Outcome:

Disease detection rate

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

照明闪烁时间范围

指标类型:

次要指标

Outcome:

Lighting flash time range

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

受检者总体检查舒适度

指标类型:

次要指标

Outcome:

Overall comfort of the subjects

Type:

Secondary 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:

N/A

Tissue:

人体标本去向

其它  

说明

无标本采集

Fate of sample:

0thers  

Note:

No samples were collected

征募研究对象情况:

Recruiting status:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age 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):

不适用

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

N/A

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:

不适用

Blinding:

N/A

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):

于项目完成后6个月公开于本平台

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

6 months after the completion of the project on this platform

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:

使用纸质病例报告表

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

Using paper case record form

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2021-01-21 12:21:23