ChiCTR1800019763 版本V1.2 版本创建时间2019/08/04 16:56:52 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:

ChiCTR1800019763 

最近更新日期:

Date of Last Refreshed on:

2019-08-04 16:56:22 

注册时间:

Date of Registration:

2018-11-27 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

纳布啡与芬太尼在ICU非机械通气患者中的应用

Public title:

The Application of nalbuphine and fentanyl in patients with non-mechanical ventilation in ICU

注册题目简写:

English Acronym:

研究课题的正式科学名称:

纳布啡与芬太尼在ICU非机械通气患者中的应用

Scientific title:

The Application of nalbuphine and fentanyl in patients with non-mechanical ventilation in ICU

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:

赵瑞巧 

研究负责人:

孙同文 

Applicant:

Ruiqiao Zhao 

Study leader:

Tongwen Sun 

申请注册联系人电话:

Applicant telephone:

+86 18837125393

研究负责人电话:

Study leader's telephone:

+86 13838516919

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:

zhaoruiqiao2017@163.com

研究负责人电子邮件:

Study leader's E-mail:

suntongwen@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:

河南省郑州市二七区建设东路1号

研究负责人通讯地址:

河南省郑州市二七区建设东路1号

Applicant address:

1 Jianshe Road East, Erqi District, Zhengzhou, He'nan, China

Study leader's address:

1 Jianshe Road East, Erqi District, Zhengzhou, He'nan, 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:

郑州大学第一附属医院

Applicant's institution:

The First Affiliated Hospital of Zhengzhou University

研究负责人所在单位:

郑州大学第一附属医院

Affiliation of the Leader:

The First Affiliated Hospital of Zhengzhou University

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:

SS-2018-41

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:

郑州大学第一附属医院科研和临床试验伦理委员会

Name of the ethic committee:

the Ethics Committee of Scientific Research and Clinical Trial of the First Affiliated Hospital of Zhengzhou University

伦理委员会批准日期:

Date of approved by ethic committee:

2018-11-07 00:00:00

伦理委员会联系人:

田丽

Contact Name of the ethic committee:

Li Tian

伦理委员会联系地址:

河南省郑州市二七区建设东路1号

Contact Address of the ethic committee:

1 Jianshe Road East, Erqi District, Zhengzhou, He'nan, 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:

郑州大学第一附属医院

Primary sponsor:

The First Affiliated Hospital of Zhengzhou University

研究实施负责(组长)单位地址:

河南省郑州市二七区建设东路1号

Primary sponsor's address:

1 Jianshe Road East, Erqi District, Zhengzhou, He'nan, 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):

河南省

市(区县):

郑州市

Country:

China

Province:

He'nan

City:

Zhengzhou

单位(医院):

郑州大学第一附属医院

具体地址:

河南省郑州市二七区建设东路1号

Institution
hospital:

The First Affiliated Hospital of Zhengzhou University

Address:

1 Jianshe Road East, Erqi District, Zhengzhou, He'nan, China

国家:

中国

省(直辖市):

山东省

市(区县):

青岛市

Country:

China

Province:

Shandong

City:

Qingdao

单位(医院):

青岛大学附属医院

具体地址:

青岛市市南区江苏路16号

Institution
hospital:

The Affiliated Hospital of Qingdao University

Address:

No. 16 Jiangsu Road, Shinan District, Qingdao

经费或物资来源:

河南省卫生计生科技创新型人才“51282”工程,部分自筹

Source(s) of funding:

He'nan Province Health and Family Planning Technology Innovation Talents

Target disease:

patients with non-mechanical ventilation in ICU

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:

比较纳布啡与芬太尼在ICU非机械通气患者中的安全性及有效性  

Objectives of Study:

Comparison of safety and efficacy of nalbuphine and fentanyl in patients with non-mechanical ventilation in ICU

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、CPOT评分>=3分;
2、ICU非有创机械通气人群;
3、年龄>18岁和<75岁;

Inclusion criteria

1. CPOT scores>=3 points;
2. patients with non-mechanical ventilation in ICU;
3. Aged 18 to 75 years old.

排除标准:

1、年龄小于18岁,或年龄大于75岁;2、妊娠或哺乳 ;3、48小时内需全麻外科手术者;4、严重的、已存在的实质性肝病伴临床显著的门静脉高压、Child-Pugh C级肝硬化或急性肝衰竭;5、支气管哮喘或COPD,重症肌无力患者;6、严重颅脑损伤,脑肿瘤,颅内压增高等易陷入呼吸抑制患者;7、有酒精或药物滥用史的患者;8、任何妨碍正确评估认知功能的情况,如语言和感觉障碍或精神障碍(语言困难或精神器质性功能障碍);9、无法获得知情同意或授权;10、筛查前6个月内参加其他探索性临床试验;11、对纳布啡或芬太尼过敏;

Exclusion criteria:

1. Pregnancy or lactation;
2. general anesthesia surgeon within 48 hours;
3. Severe, existing substantial liver disease with clinically significant portal hypertension, Child-Pugh C cirrhosis or acute liver failure;
4. bronchial asthma or COPD, myasthenia gravis patients;
5. severe craniocerebral injury, brain tumor, increased intracranial pressure and other susceptible to respiratory depression in patients;
6. patients with a history of alcohol or drug abuse;
7. Any condition that prevents proper assessment of cognitive function, such as language and sensory impairment or mental disorder (language difficulties or mental organic dysfunction);
8. unable to obtain informed consent or authorization;
9. participate in other exploratory clinical trials within 6 months prior to screening;
10. allergic to nalbuphine or fentanyl.

研究实施时间:

Study execute time:

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

征募观察对象时间:

Recruiting time:

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

干预措施:

Interventions:

组别:

纳布啡组

样本量:

150

Group:

Group 1

Sample size:

干预措施:

负荷剂量0.1mg/kg静脉推注(时间大于1分钟),然后以0.05mg/kg/h持续泵入(50mg加生理盐水至50ml,3ml/h),最大泵入速度为0.2mg/kg/h(12ml/h)

干预措施代码:

Intervention:

Nalbuphine

Intervention code:

组别:

芬太尼组

样本量:

150

Group:

Group 2

Sample size:

干预措施:

负荷剂量0.03ug/kg(时间大于1分钟),然后以0.5ug/kg/h持续泵入(500ug加生理盐水至50ml,3ml/h),最大泵入速度为2ug/kg/h

干预措施代码:

Intervention:

Fentanyl

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

河南省 

市(区县):

郑州市 

Country:

China 

Province:

He'nan 

City:

Zhengzhou 

单位(医院):

郑州大学第一附属医院 

单位级别:

三级甲等 

Institution
hospital:

The First Affiliated Hospital of Zhengzhou University

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

山东省 

市(区县):

青岛市 

Country:

China 

Province:

Shandong 

City:

Qingdao 

单位(医院):

青岛大学附属医院 

单位级别:

三级甲等 

Institution
hospital:

The Affliliated Hospital of Qingdao University

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

河南省 

市(区县):

信阳市 

Country:

China 

Province:

He'nan 

City:

Xinyang 

单位(医院):

信阳市中心医院 

单位级别:

三级甲等 

Institution
hospital:

Xinyang Central Hospital

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

贵州省 

市(区县):

遵义市 

Country:

China 

Province:

Guizhou 

City:

Zunyi 

单位(医院):

遵义医学院附属医院 

单位级别:

三级甲等 

Institution
hospital:

Affiliated Hospital of Zunyi Medical College

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

广东省 

市(区县):

深圳市 

Country:

China 

Province:

Guangdong 

City:

 

单位(医院):

深圳市宝安区人民医院 

单位级别:

三级甲等 

Institution
hospital:

The People's Hospital of Baoan Shenzhen

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

湖北省 

市(区县):

武汉市 

Country:

China 

Province:

Hubei 

City:

Wuhan 

单位(医院):

武汉大学人民医院 

单位级别:

三级甲等 

Institution
hospital:

Renmin Hospital of Wuhan University

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

湖北省 

市(区县):

武汉市 

Country:

China 

Province:

Hubei 

City:

Wuhan 

单位(医院):

武汉协和医院 

单位级别:

三级甲等 

Institution
hospital:

Wuhan Union Hospital

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

云南省 

市(区县):

昆明市 

Country:

China 

Province:

Yunnan 

City:

Kunming 

单位(医院):

昆明医科大学第一附属医院 

单位级别:

三级甲等 

Institution
hospital:

First Affiliated Hospital of Kunming Medical University

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

河南省 

市(区县):

郑州市 

Country:

China 

Province:

He'nan 

City:

Zhengzhou 

单位(医院):

河南省人民医院 

单位级别:

三级甲等 

Institution
hospital:

Henan Provincial People's Hospital

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

河南省 

市(区县):

郑州市 

Country:

China 

Province:

He'nan 

City:

Zhengzhou 

单位(医院):

郑州大学第二附属医院 

单位级别:

三级甲等 

Institution
hospital:

The Second Affiliated Hospital of Zhengzhou University

Level of the institution:

Tertiary A Hospital

测量指标:

Outcomes:

指标中文名:

重症监护疼痛观察量表

指标类型:

主要指标

Outcome:

CPOT score

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

Richmond 躁动 - 镇静评分

指标类型:

次要指标

Outcome:

RASS score

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

ICU 患者意识模糊评估法

指标类型:

次要指标

Outcome:

CAM-ICU score

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

不良反应发生率

指标类型:

次要指标

Outcome:

Incidence of adverse reactions

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

APACHEII评分

指标类型:

次要指标

Outcome:

APACHEII score

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

SOFA评分

指标类型:

次要指标

Outcome:

SOFA score

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

生化指标

指标类型:

次要指标

Outcome:

biochemical index

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血常规

指标类型:

次要指标

Outcome:

routine blood examination

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

动脉血气分析

指标类型:

次要指标

Outcome:

arterial blood gas analysis

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:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 75 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):

计算机产生随机数法

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

Ivestigators/ by a computer-based random-number generator

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:

未说明

Blinding:

Not stated

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):

以发表论文形式公开。网络平台为中国临床试验注册中心(网址:http://www.chictr.org.cn)

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

Publish paper. China Clinical Trial Registry (网址:http://www.chictr.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:

病例记录表

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

CRF

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:

 2018-11-27 22:28:14