|
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: |
|
||||||||||||||||||||||||||||||||||||||||||||
|
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; |
||||||||||||||||||||||||||||||||||||||||||||
|
Inclusion criteria |
1. CPOT scores>=3 points; |
||||||||||||||||||||||||||||||||||||||||||||
|
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; |
||||||||||||||||||||||||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2018-12-01 00:00:00至 To 2019-12-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2018-12-01 00:00:00 至 To 2019-12-01 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
正在进行 Recruiting |
年龄范围: Participant age: |
|
||||||
|
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
|
|
|
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 |