ChiCTR2400090608 版本V1.0 版本创建时间2024/10/09 17:48:24 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:

ChiCTR2400090608 

最近更新日期:

Date of Last Refreshed on:

2024-10-09 17:48:17 

注册时间:

Date of Registration:

2024-10-09 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

脓毒症等重症感染相关凝血病临床特征研究

Public title:

Clinical Features of Coagulopathy Associated with Sepsis and other severe infection

注册题目简写:

English Acronym:

研究课题的正式科学名称:

脓毒症等重症感染相关凝血病临床特征研究

Scientific title:

Clinical Features of Coagulopathy Associated with Sepsis

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:

陈广 

研究负责人:

宁琴 

Applicant:

Chen Guang 

Study leader:

Qin Ning 

申请注册联系人电话:

Applicant telephone:

+86 181 0860 2825

研究负责人电话:

Study leader's telephone:

+86 27 8366 2391

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:

chenguang@tjh.tjmu.edu.cn

研究负责人电子邮件:

Study leader's E-mail:

qning@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:

湖北省武汉市解放大道1095号同济医院感染科

研究负责人通讯地址:

湖北省武汉市解放大道1095号同济医院感染科

Applicant address:

1095 Jiefang Avenue, Hankou, Wuhan, China

Study leader's address:

1095 Jiefang Avenue, Hankou, Wuhan, 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:

华中科技大学同济医学院附属同济医院

Applicant's institution:

Tongji Hospital of 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同济医院

Affiliation of the Leader:

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

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:

TJ-IRB202405032

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同济医院医学伦理委员会

Name of the ethic committee:

Medical Ethics Committee of Tongji 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:

2024-05-31 00:00:00

伦理委员会联系人:

周璞

Contact Name of the ethic committee:

Zhou Pu

伦理委员会联系地址:

湖北省武汉市解放大道1095号华中科技大学同济医学院附属同济医院科研处

Contact Address of the ethic committee:

1095 Jiefang Avenue, Hankou, Wuhan, China Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 27 8366 3940

伦理委员会联系人邮箱:

Contact email of the ethic committee:

tongjilunli@163.com

研究实施负责(组长)单位:

华中科技大学同济医学院附属同济医院

Primary sponsor:

Tongji Hospital of 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1095号同济医院

Primary sponsor's address:

1095 Jiefang Avenue, Hankou, Wuhan, China

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):

Country:

China

Province:

HuBei

City:

单位(医院):

华中科技大学同济医学院附属同济医院

具体地址:

湖北省武汉市解放大道1095号同济医院

Institution
hospital:

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

Address:

1095 Jiefang Avenue, Hankou, Wuhan, China

经费或物资来源:

研究者自筹经费

Source(s) of funding:

Investigator-initiated funding

Target disease:

sepsis

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:

队列研究 

Study design:

Cohort study 

研究目的:

通过真实世界研究,分析研究脓毒症等重症感染相关凝血病临床特征,建立脓毒症相关凝血病分期指标量化诊断体系;建立脓毒症相关凝血病预后预测模型,并探索脓毒症相关凝血病不同时相治疗方案.  

Objectives of Study:

Through real-world studies, analyze the clinical characteristics of coagulopathy associated with sepsis and other severe infections, establish a quantitative diagnostic system for staging indicators of sepsis-related coagulopathy; establish a prognostic prediction model for sepsis-related coagulopathy, and explore treatment plans for sepsis-related coagulopathy at different stages

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

脓毒症等重症感染患者,入院时或住院期间,满足下列条件中的①②,伴或不伴③④ ① 体温>38℃或<36℃ ② 外周血白细胞计数大于12×109/L或低于4×109/L ③ 心率>90次/分或低血压(收缩压<90 mmHg,或较基线降低>40 mmHg)。 ④ 呼吸急促(>20次/分)或通气过度(PaCO2<32mmHg)。

Inclusion criteria

For patients with sepsis and other severe infections, upon admission or during hospitalization, if they meet conditions ① and ②, with or without ③ and ④: ① Body temperature >38°C or <36°C ② Peripheral white blood cell count greater than 12×10^9/L or less than 4×10^9/L ③ Heart rate >90 beats per minute or hypotension (systolic blood pressure <90 mmHg, or a decrease of >40 mmHg from baseline). ④ Rapid breathing (>20 breaths per minute) or hyperventilation (PaCO2 <32 mmHg).

排除标准:

1) 合并肿瘤,包括血液系统肿瘤及实体瘤等; 2) 风湿结缔组织疾病; 3) 先天性凝血障碍性疾病:血友病甲、乙、丙;血管性假血友病;凝血因子缺乏性疾病(Ⅰ、Ⅱ、Ⅴ、Ⅶ、Ⅹ、Ⅺ、Ⅻ、ⅩⅢ、激肽释放酶原等存在先天性缺乏症); 4) 合并其它基础疾病,目前使用肝素、华法林、口服新型抗凝药、抗血小板药物等抗凝治疗药物; 5) 2周内接受大型手术治疗等; 6) 患者本人或授权委托人无法签署或拒绝签署知情同意书

Exclusion criteria:

1) Coexisting malignancies, including hematological tumors and solid tumors; 2) Rheumatic connective tissue diseases; 3) Congenital coagulation disorders: Hemophilia A, B, C; Von Willebrand disease; Deficiencies of coagulation factors (congenital deficiencies of factors Ⅰ, Ⅱ, Ⅴ, Ⅶ, Ⅹ, Ⅺ, Ⅻ, ⅩⅢ, and prekallikrein); 4) Concurrent other underlying diseases, currently using anticoagulant drugs such as heparin, warfarin, oral novel anticoagulants, antiplatelet agents, etc.; 5) Received major surgery within the past 2 weeks; 6) The patient or authorized representative is unable to sign or refuses to sign the informed consent form.

研究实施时间:

Study execute time:

From 2024-10-10 00:00:00 To 2026-10-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2024-10-10 00:00:00 To 2026-10-31 00:00:00  

干预措施:

Interventions:

组别:

观察性研究

样本量:

600

Group:

Observational study

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):

湖北省 

市(区县):

 

Country:

China 

Province:

Hubei 

City:

 

单位(医院):

华中科技大学同济医学院附属同济医院 

单位级别:

三甲 

Institution
hospital:

Tongji Hospital of 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:

脓毒症等重症感染相关凝血病临床特征

指标类型:

主要指标

Outcome:

clinical features of sepsis and other severe infection-related coagulopathy

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

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

标本中文名:

尿液

组织:

Sample Name:

Urine

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction 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 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):

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

none

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:

病例记录表

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

Case Record 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:

 2024-10-09 17:48:17