ChiCTR2100045892 版本V1.0 版本创建时间2021/04/27 01:27:36 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:

ChiCTR2100045892 

最近更新日期:

Date of Last Refreshed on:

2021-04-27 01:26:00 

注册时间:

Date of Registration:

2021-04-27 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

注射用重组人尿激酶原在冠状动脉腔内注入后对ST段抬高型心肌梗死患者的临床观察

Public title:

Clinical observation on patients with ST-segment elevation myocardial infarction after injection of recombinant human prourokinase into coronary artery

注册题目简写:

English Acronym:

研究课题的正式科学名称:

注射用重组人尿激酶原在冠状动脉腔内注入后对ST段抬高型心肌梗死患者的临床观察

Scientific title:

Clinical observation on patients with ST-segment elevation myocardial infarction after injection of recombinant human prourokinase into coronary artery

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:

王子超 

研究负责人:

王子超 

Applicant:

Wang Zichao 

Study leader:

Wang Zichao 

申请注册联系人电话:

Applicant telephone:

+86 15847219898

研究负责人电话:

Study leader's
telephone:

+86 15847219898

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:

wzch721030@163.com

研究负责人电子邮件:

Study leader's E-mail:

wzch721030@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:

内蒙古包头市青山区呼得木林大街30号

研究负责人通讯地址:

内蒙古包头市青山区呼得木林大街30号

Applicant address:

30 Hudemulin Street, Baotou, Inner Mongolia Autonomous Region, China

Study leader's address:

30 Hudemulin Street, Baotou, Inner Mongolia Autonomous Region, 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:

内蒙古科技大学包头医学院第二附属医院

Applicant's institution:

The Second Affiliated Hospital of Inner Mongolia University of Science and Technology Baotou Medical College

研究负责人所在单位:

内蒙古科技大学包头医学院第二附属医院

Affiliation of the Leader:

The Second Affiliated Hospital of Inner Mongolia University of Science and Technology Baotou Medical College

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:

2X-038

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:

包头医学院第二附属医院伦理委员会

Name of the ethic committee:

The Second Affiliated Hospital of Baotou Medical College Ethics Committee

伦理委员会批准日期:

Date of approved by ethic committee:

1990-01-01 00:00:00

伦理委员会联系人:

桂艳霞

Contact Name of the ethic committee:

Gui Yanxia

伦理委员会联系地址:

内蒙古包头市青山区呼得木林大街30号

Contact Address of the ethic committee:

30 Hudemulin Street, Baotou, Inner Mongolia Autonomous Region, 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:

内蒙古科技大学包头医学院第二附属医院

Primary sponsor:

The Second Affiliated Hospital of Inner Mongolia University of Science and Technology Baotou Medical College

研究实施负责(组长)单位地址:

内蒙古包头市青山区呼得木林大街30号

Primary sponsor's address:

30 Hudemulin Street, Baotou, Inner Mongolia Autonomous Region, 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):

内蒙古

市(区县):

包头

Country:

China

Province:

Inner Mongolia Autonomous Region

City:

Baotou

单位(医院):

内蒙古科技大学包头医学院第二附属医院

具体地址:

内蒙古包头市青山区呼得木林大街30号

Institution
hospital:

The Second Affiliated Hospital of Inner Mongolia University of Science and Technology Baotou Medical College

Address:

30 Hudemulin Street

经费或物资来源:

包头市医药卫生科技计划项目Wsjj2018094

Source(s) of funding:

Baotou City Medical and Health Science and Technology Plan Project Wsjj2018094

研究疾病:

ST段抬高型心肌梗死  

Target disease:

ST-segment elevation myocardial infarction

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:

治疗新技术临床试验 

Study phase:

New Treatment Measure Clinical Study

研究设计:

非随机对照试验 

Study design:

Non randomized control 

研究目的:

探讨在急性ST段抬高型心肌梗死患者冠状动脉内给予重组人尿激酶原,对患者冠状动脉介入术中血管再通的影响及其安全性。  

Objectives of Study:

To investigate the effect and safety of Recombinant Human Prourokinase in the coronary arteries of patients with STEMI on recanalization during coronary intervention.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

所有入选患者均符合《急性ST段抬高型心肌梗死诊断和治疗指南》中的急性ST段抬高型心肌梗死的诊断标准:
(1)有明显的心肌缺血症状;
(2)新出现的或怀疑为新出现的心电图上明显的ST-T改变或新出现的左束支传导阻滞,以及新出现的病理性Q波;
(3)心肌损伤标志物浓度的改变。

Inclusion criteria

All selected patients met the diagnostic criteria for acute ST-segment elevation myocardial infarction in the Guidelines for the Diagnosis and Treatment of Acute ST-segment Elevation Myocardial Infarction:
(1) There are obvious symptoms of myocardial ischemia
(2) Newly-appearing or suspected to be newly-appearing obvious ST-T changes on the ECG or newly-appearing left bundle branch block, and newly-appearing pathological Q waves;
(3) Changes in the concentration of myocardial injury markers.

排除标准:

(1)近期有出血史、创伤史、内脏手术史及脑出血史等;
(2)存在严重肝肾功能不全;
(3)合并肿瘤;
(4)有出血倾向或有出血性疾病者;
(5)对研究药物及碘剂过敏者;
(6)妊娠期患者;
(7)存在难以控制的严重高血压(≥180/110mmHg)和急性心力衰竭者;
(8)既往行冠脉支架植入术或冠脉搭桥者;
(9)正在参与其他临床试验者。

Exclusion criteria:

(1) Recent history of bleeding, trauma, visceral surgery and cerebral hemorrhage, etc.;
(2) There is severe liver and kidney dysfunction;
(3) Combined tumor;
(4) People with bleeding tendency or bleeding diseases;
(5) Those who are allergic to research drugs and iodine;
(6) Patients during pregnancy;
(7) Those with severe hypertension (≥180/110mmHg) and acute heart failure that are difficult to control;
(8) Those who underwent coronary stent implantation or coronary artery bypass graft in the past;
(9) Those who are participating in other clinical trials.

研究实施时间:

Study execute time:

From 2018-01-01 00:00:00 To 2019-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2018-03-01 00:00:00 To 2019-07-31 00:00:00

干预措施:

Interventions:

组别:

试验组

样本量:

55

Group:

Experimental group

Sample size:

干预措施:

重组人尿激酶原

干预措施代码:

Intervention:

recombinant human prourokinase

Intervention code:

组别:

对照组

样本量:

53

Group:

Control group

Sample size:

干预措施:

干预措施代码:

Intervention:

nothing

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

内蒙古自治区 

市(区县):

包头 

Country:

China

Province:

Inner Mongolia Autonomous Region

City:

Baotou

单位(医院):

内蒙古科技大学包头医学院第二附属医院 

单位级别:

三级 

Institution
hospital:

The Second Affiliated Hospital of Inner Mongolia University of Science and Technology Baotou Medical College

Level of the institution:

Tertiary

测量指标:

Outcomes:

指标中文名:

ST段回落水平

指标类型:

主要指标

Outcome:

ST resolution

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

左室射血分数

指标类型:

主要指标

Outcome:

Left Ventricular Ejection Fractions, LVEF

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

左室舒张末期内径

指标类型:

主要指标

Outcome:

left ventricular end-diastolic dimension, LVDD

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

主要不良心血管事件

指标类型:

主要指标

Outcome:

major adverse cardiovascular events

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:

肌酸激酶同工酶

组织:

Sample Name:

MB isoenzyme

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:

肌钙蛋白 I

组织:

Sample Name:

troponin I

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:

结束

/Completed

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):

由主要研究者以随机数字法获得随机序列

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

The random sequence was obtained by random number method by the primary researcher

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

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):

2021年,中国临床试验注册中心,http://www.chictr.cn/edit.aspx

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

2021,China clinical trial registry,http://www.chictr.cn/edit.aspx

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:

EXCEL,SPSS

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

EXCEL,SPSS

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2021-04-27 01:26:00