心脏移植慢性排斥反应多模态影像评估及预后分析

注册号:

Registration number:

ChiCTR2100047545 

最近更新日期:

Date of Last Refreshed on:

2022-02-20 17:52:46 

注册时间:

Date of Registration:

2021-06-20 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

心脏移植慢性排斥反应多模态影像评估及预后分析

Public title:

Multimodal imaging evaluation of chronic rejection of heart transplantation and prognostic analysis

注册题目简写:

English Acronym:

研究课题的正式科学名称:

心脏移植慢性排斥反应多模态影像评估及预后分析

Scientific title:

Multimodal imaging evaluation of chronic rejection of heart transplantation and prognostic analysis

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:

朱双双 

研究负责人:

张丽 

Applicant:

Zhu Shuangshuang 

Study leader:

Zhang Li 

申请注册联系人电话:

Applicant telephone:

+86 15971428009

研究负责人电话:

Study leader's
telephone:

+86 18907131488

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:

18846032209@163.com

研究负责人电子邮件:

Study leader's E-mail:

zli429@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:

湖北省武汉市江汉区解放大道1277号

研究负责人通讯地址:

湖北省武汉市江汉区解放大道1277号

Applicant address:

1277 Jiefang Avenue, Jianghan District, Wuhan, Hubei

Study leader's address:

1277 Jiefang Avenue, Jianghan District, 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:

No

伦理委员会批件文号:

Approved No. of ethic committee:

伦理委员会批件附件:

Approved file of Ethical Committee:

批准本研究的伦理委员会名称:

Name of the ethic committee:

伦理委员会批准日期:

Date of approved by ethic committee:

2013-08-26 00:00:00

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:

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:

湖北省武汉市江汉区解放大道1277号

Primary sponsor's address:

1277 Jiefang Avenue, Jianghan District, 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:

江汉区解放大道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:

湖北省重点研发计划项目

Source(s) of funding:

Key R&D Projects in Hubei Province

研究疾病:

心脏移植  

Target disease:

Heart transplantation

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:

连续入组 

Study design:

Sequential 

研究目的:

本项目拟联合多模态影像技术,筛选准确预测HT术后慢性排斥反应的无创影像学参数,构建HT术后不良结局的风险预测系统,并通过临床研究进一步明确其有效性。  

Objectives of Study:

This project plans to combine multimodal imaging technology to screen non-invasive imaging parameters that accurately predict chronic rejection after HT, build a risk prediction system for adverse outcomes after HT, and further clarify its effectiveness through clinical research.

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.严重心肺病;
2.中度至重度慢性肾脏患者;
3.怀孕,可能怀孕或哺乳期的患者;
4.研究者或研究者认为不适合参加本研究的患者。

Exclusion criteria:

1.Severe heart and lung disease;
2.Patients with moderate to severe chronic kidney disease;
3.Patients who are pregnant, possibly pregnant or breast-feeding;
4.Researchers or patients deemed unsuitable to participate in this study.

研究实施时间:

Study execute time:

From 2021-05-22 00:00:00 To 2023-06-30 00:00:00  

征募观察对象时间:

Recruiting time:

From 2021-06-21 00:00:00 To 2023-06-30 00:00:00

干预措施:

Interventions:

组别:

连续入组

样本量:

200

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):

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:

三级甲等 

Institution
hospital:

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

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

冠状动脉血管狭窄程度

指标类型:

主要指标

Outcome:

Coronary artery stenosis degree

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

超声应变参数

指标类型:

主要指标

Outcome:

Ultrasonic strain parameters

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

心肌纤维化参数

指标类型:

主要指标

Outcome:

Myocardial fibrosis parameters

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

其它  

说明

Fate of sample:

0thers  

Note:

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 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):

无。

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:

N/A

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):

未说明 请阅读网页注册指南中关于“原始数据共享”的内容。

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

Not stated

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:

使用临床试验公共管理平台。

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

Using clinical trial management public platform.

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2021-06-20 05:58:15