ChiCTR2000034594 版本V1.0 版本创建时间2020/07/11 21:43:25 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:

ChiCTR2000034594 

最近更新日期:

Date of Last Refreshed on:

2020-07-11 21:43:20 

注册时间:

Date of Registration:

1990-01-01 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

章艺医师:该研究尚未获得伦理委员会批准,请于批准后再开始纳入参试者,并与我们联系上传批件。 尼可地尔对脓毒症休克患者肾脏保护的临床研究

Public title:

Effects of nicorandil on real function in septic shock patients

注册题目简写:

English Acronym:

研究课题的正式科学名称:

尼可地尔对脓毒症休克患者肾脏保护的临床研究

Scientific title:

尼可地尔对脓毒症休克患者肾脏保护的临床研究

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:

章艺 

研究负责人:

赵文静 

Applicant:

Yi Zhang 

Study leader:

Wenjing Zhao 

申请注册联系人电话:

Applicant telephone:

13092355769

研究负责人电话:

Study leader's telephone:

13852157285

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:

1137266193@qq.com

研究负责人电子邮件:

Study leader's E-mail:

Zhaowj886@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:

江苏省徐州市泉山区淮海西路84号

研究负责人通讯地址:

江苏省徐州市泉山区淮海西路99号

Applicant address:

84 Huaihai Road West, Quanshan District, Xuzhou, Jiangsu, China

Study leader's address:

99 Huaihai Road West, Quanshan District, Xuzhou, Jiangsu, 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:

徐州医科大学附属医院

Applicant's institution:

Affiliated Hospital of Xuzhou Medical University

研究负责人所在单位:

Affiliation of the Leader:

是否获伦理委员会批准:

否/No

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:

徐州医科大学附属医院

Primary sponsor:

Affiliated Hospital of Xuzhou Medical University

研究实施负责(组长)单位地址:

江苏省徐州市泉山区淮海西路99号

Primary sponsor's address:

99 Huaihai Road West, Quanshan District, Xuzhou, Jiangsu, 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):

江苏

市(区县):

徐州

Country:

China

Province:

Jiangsu

City:

Xuzhou

单位(医院):

徐州医科大学附属医院

具体地址:

泉山区淮海西路99号

Institution
hospital:

Affiliated Hospital of Xuzhou Medical University

Address:

99 Huaihai Road West, Quanshan District

经费或物资来源:

Source(s) of funding:

none

Target disease:

septic shock

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

探索性研究/预试验 

Study phase:

0

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

探究尼可地尔能否改善脓毒症休克患者的肾功能,降低急性肾损伤的发生率  

Objectives of Study:

To explore whether Nicorandil can improve renal function and reduce the incidence of acute kidney injury in septic shock patients

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.我院ICU收治的患者诊断为早期(≤24 小时)脓毒性休克,参照 2016 年sepsis3.0 的定义和 2016 年拯救脓毒症运动指南诊断脓毒症休克;由2个及以上主治以上临床医师共同诊断;即脓毒症伴持续性低血压,需要血管加压药维持平均动脉压(MAP)≥65 mmHg,并且尽管有足够的液体复苏,但血清乳酸水平> 2 mmol / L?;2.患者及家属对此研究表示知情并同意。

Inclusion criteria

Patients admitted to the ICU of our hospital were diagnosed as early septic shock (≤24 hours), and sepsis shock was diagnosed according to the definition of sepsis3.0 in 2016 and the guidelines of the campaign to SSC 2016. Diagnosis shall be made jointly by 2 or more attending and above clinicians; In other words, sepsis with persistent hypotension requires vasopressors to maintain mean arterial pressure (MAP) ≥65 mmHg, and serum lactic acid level > 2 mmol/L despite adequate fluid resuscitation. Patients and their families were informed and consented to the study.

排除标准:

1.入ICU治疗前患者已存在肾功能不全;
2.入ICU治疗前患者已应用RRT治疗;
3.入 ICU7天内患者治疗中断或出院、死亡;
4.其他疾病导致的慢性肾功能不全(糖尿病、免疫性)及肾移植术后患者;
5.孕妇,哺乳期妇女、 恶性肿瘤患者及3个月内应用免疫抑制剂治疗患者。

Exclusion criteria:

1.The patient had renal insufficiency before ICU treatment.
2.Patients were treated with RRT before ICU admission.
3.Treatment interruption or discharge or death within 7 days after admission to ICU;
4.Chronic renal insufficiency (diabetes mellitus, immunity) caused by other diseases and patients after kidney transplantation;
5.Pregnant women, lactating women, patients with malignant tumor and patients treated with immunosuppressive agents within 3 months.

研究实施时间:

Study execute time:

From 2020-08-01 00:00:00 To 2021-03-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2020-08-01 00:00:00 To 2021-03-31 00:00:00  

干预措施:

Interventions:

组别:

试验组

样本量:

64

Group:

experimental group

Sample size:

干预措施:

静脉泵注尼可地尔

干预措施代码:

Intervention:

Intravenous injection of Nicorandil

Intervention code:

组别:

对照组

样本量:

64

Group:

control group

Sample size:

干预措施:

静脉泵注生理盐水

干预措施代码:

Intervention:

Intravenous injection of 0.9%NS

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

江苏 

市(区县):

徐州 

Country:

China 

Province:

Jiangsu 

City:

Xuzhou 

单位(医院):

徐州医科大学附属医院 

单位级别:

三级甲等 

Institution
hospital:

Affiliated Hospital of Xuzhou Medical University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

中性粒细胞明胶酶相关脂质运载蛋白

指标类型:

主要指标

Outcome:

NGAL

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

肾功能(肌酐,尿素氮,胱抑素C)

指标类型:

次要指标

Outcome:

renal function (serum creatinine, blood urea nitrogen, Cystatin C)

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

感染程度

指标类型:

次要指标

Outcome:

Infection degree

Type:

Secondary indicator

测量时间点:

测量方法:

降钙素;血乳酸

Measure time point of outcome:

Measure method:

procalcitonin, Lac

指标中文名:

疾病严重程度

指标类型:

次要指标

Outcome:

severity of disease

Type:

Secondary indicator

测量时间点:

测量方法:

序贯多器官功能障碍评分, 急性生理和慢性健康评分II

Measure time point of outcome:

Measure method:

sequential organ failure assessment, acute physiology and chronic health evaluation II.

指标中文名:

治疗7天使用RRT率

指标类型:

次要指标

Outcome:

RRT use rate in 7 days of treatment

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

平均ICU治疗时间

指标类型:

次要指标

Outcome:

Average ICU treatment time

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

28天病死率

指标类型:

次要指标

Outcome:

28-day mortality

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:

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:

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):

研究人员使用随机数表方法生成了随机序列。

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

研究人员使用随机数表方法生成了随机序列。

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

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):

书面审理后六个月内;ResMan, http://www.medresman.org.cn。

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

Within six months after the trial complete by paper; ResMan, http://www.medresman.org.cn.

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:

Within six months after the trial complete by paper; ResMan, http://www.medresman.org.cn.

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

1. Clinical data collection uses Case Record Form (CRF); 2. Data collection and management system with Electronic Data Capture(EDC

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2020-07-11 21:43:20