血必净在急性腹膜炎致脓毒症中的免疫调控作用

注册号:

Registration number:

ChiCTR1900020593 

最近更新日期:

Date of Last Refreshed on:

2019-01-09 18:54:50 

注册时间:

Date of Registration:

2019-01-09 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

血必净在急性腹膜炎致脓毒症中的免疫调控作用

Public title:

Effect of Xuebijing injection on macrophage polarization in patients with peritonitis-induced sepsis

注册题目简写:

English Acronym:

研究课题的正式科学名称:

血必净在急性腹膜炎致脓毒症中的免疫调控作用

Scientific title:

Effect of Xuebijing injection on macrophage polarization in patients with peritonitis-inducede 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:

李锦媛 

研究负责人:

赵泉 

Applicant:

Jinyuan Li 

Study leader:

Quan Zhao 

申请注册联系人电话:

Applicant telephone:

+86 13529132284

研究负责人电话:

Study leader's
telephone:

+86 13759579998

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:

jinyuan1208@126.com

研究负责人电子邮件:

Study leader's E-mail:

13759579998@163.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:

云南省昆明市金碧路157号

研究负责人通讯地址:

云南省昆明市金碧路157号

Applicant address:

157 Jinbi Road, Kunming, Yunnan, China

Study leader's address:

157 Jinbi Road, Kunming, Yunnan, China

申请注册联系人邮政编码:

Applicant postcode:

650032

研究负责人邮政编码:

Study leader's postcode:

申请人所在单位:

云南省第一人民医院

Applicant's institution:

the First People's Hospital of Yunnan Province

研究负责人所在单位:

云南省第一人民医院

Affiliation of the Leader:

the First People's Hospital of Yunnan Province

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:

KHLL2018-KY063

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:

云南省第一人民医院医学伦理委员会

Name of the ethic committee:

the First People's Hospital of Yunnan Province Ethic Committee

伦理委员会批准日期:

Date of approved by ethic committee:

2018-12-26 00:00:00

伦理委员会联系人:

李蓉

Contact Name of the ethic committee:

Rong Li

伦理委员会联系地址:

云南省昆明市金碧路157号

Contact Address of the ethic committee:

157 Jinbi Road, Kunming, Yunnan, China

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:

云南省第一人民医院

Primary sponsor:

the First People's Hospital of Yunnan Province

研究实施负责(组长)单位地址:

云南省昆明市金碧路157号

Primary sponsor's address:

157 Jinbi Road, Kunming, Yunnan, 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):

云南

市(区县):

Country:

China

Province:

Yunnan

City:

单位(医院):

云南省第一人民医院

具体地址:

云南省昆明市金碧路157号

Institution
hospital:

the First People's Hospital of Yunnan Province

Address:

157 Jinbi Road, Kunming, Yunnan, China

经费或物资来源:

天津红日药业股份有限公司

Source(s) of funding:

Tianjin red sun pharmaceutical Technology

研究疾病:

腹膜炎相关脓毒症  

Target disease:

peritonitis-induced sepsis

研究疾病代码:

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

上市后药物 

Study phase:

4

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

评价常规疗法联合血必净在脓毒症免疫调节治疗中的作用  

Objectives of Study:

To evaluate effect of Xuebijing injection on macrophage polarization in patients with acute peritonitis

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)孕妇、哺乳期妇女和可能妊娠的妇女;
(2)患有影响生存的严重疾病(例如不能切除的肿瘤、血液病、 脑血管疾病导致长期卧床、老年痴呆等) ;
(3)对本药过敏者;
(4)精神疾病患者;
(5)长期使用免疫抑制药物
(6)参加多项临床试验。

Exclusion criteria:

1. Diagnosis of sepsis for more than 48 h;
2. Pregnant and lactating women;
3. Severe primary disease including unrespectable tumours, blood diseases and Human Immunodeficiency Virus (HIV);
4. Severe liver and kidney dysfunction (single liver or kidney SOFA score ≥ 3 points);
5. Use of an immunosuppressant or having an organ transplant within the previous 6 months;
6. Participating in other clinical trials in the previous 30 days.

研究实施时间:

Study execute time:

From 2019-01-20 00:00:00 To 2021-01-20 00:00:00  

征募观察对象时间:

Recruiting time:

From 2019-01-20 00:00:00 To 2020-10-31 00:00:00

干预措施:

Interventions:

组别:

实验组

样本量:

60

Group:

Experiment group

Sample size:

干预措施:

血必净+常规ICU治疗

干预措施代码:

Intervention:

Xuebijing plus routine therapy

Intervention code:

组别:

对照组

样本量:

60

Group:

Control group

Sample size:

干预措施:

常规ICU治疗

干预措施代码:

Intervention:

Routine therapy

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

云南 

市(区县):

昆明 

Country:

China

Province:

Yunnnan

City:

Kunming

单位(医院):

云南省第一人民医院 

单位级别:

三甲医院 

Institution
hospital:

the First People’s Hospital of Yunnan Province

Level of the institution:

Tertiary A Hospital

测量指标:

Outcomes:

指标中文名:

28天院内死亡率

指标类型:

主要指标

Outcome:

28-day mortality

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

炎症因子

指标类型:

次要指标

Outcome:

proinflammatory cytokines

Type:

Secondary indicator

测量时间点:

测量方法:

ELISA

Measure time point of outcome:

Measure method:

指标中文名:

抑炎因子

指标类型:

次要指标

Outcome:

Anti-inflammatory factors

Type:

Secondary indicator

测量时间点:

测量方法:

ELISA

Measure time point of outcome:

Measure method:

指标中文名:

DAO

指标类型:

次要指标

Outcome:

DAO

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

IFABP

指标类型:

次要指标

Outcome:

IFABP

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

D-乳酸

指标类型:

次要指标

Outcome:

D-lactate

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

APACHE II 评分

指标类型:

主要指标

Outcome:

APACHE II score

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):

分层随机化法

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

Stratified randomization

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:

双盲法

Blinding:

double blind

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):

ResMan

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

ResMan

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:

ResMan

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

ResMan

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:

 2019-01-09 18:54:16