ChiCTR2400087027 版本V1.0 版本创建时间2024/07/17 16:03:28 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:

ChiCTR2400087027 

最近更新日期:

Date of Last Refreshed on:

2024-07-17 16:03:16 

注册时间:

Date of Registration:

2024-07-17 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

11·(审核员标记请勿删除;如尚无参试者入组,可适当后延征募参试者时间起始时间,建议为修改完成日期之后的5天以上,以免成为补注册。请对照研究计划书补充完整测量指标,并且区分填写、确认主要/次要;)护士与病患对术后自控镇痛泵宣教认识差异的调查

Public title:

A cross-sectional study to assess the difference of perspective of postoperative patient-controlled analgesia pump information between the patients and nurses

注册题目简写:

English Acronym:

研究课题的正式科学名称:

护士与病患对术后自控镇痛泵宣教认识差异的调查

Scientific title:

A cross-sectional study to assess the difference of perspective of postoperative patient-controlled analgesia pump information between the patients and nurses

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:

石贇 

研究负责人:

胡元叶 

Applicant:

Yun Shi 

Study leader:

Yuanye Hu 

申请注册联系人电话:

Applicant telephone:

+86 139 1826 8351

研究负责人电话:

Study leader's telephone:

+86 137 6410 9313

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:

shi_yun@fudan.edu.cn

研究负责人电子邮件:

Study leader's E-mail:

imula@sohu.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:

上海市闵行区万源路399号

研究负责人通讯地址:

上海市闵行区万源路399号

Applicant address:

399 Wanyuan Road, Minhang District, Shanghai

Study leader's address:

399 Wanyuan Road, Minhang District, Shanghai

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:

复旦大学附属儿科医院

Applicant's institution:

Children's Hospital of Fudan University

研究负责人所在单位:

复旦大学附属儿科医院

Affiliation of the Leader:

Children's Hospital of Fudan 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:

复儿伦审(2024)69号

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:

复旦大学附属儿科医院伦理委员会

Name of the ethic committee:

Ethics Committee of Children's Hospital of Fudan University

伦理委员会批准日期:

Date of approved by ethic committee:

2024-04-28 00:00:00

伦理委员会联系人:

阚海东

Contact Name of the ethic committee:

Haidong Kan

伦理委员会联系地址:

上海市闵行区万源路399号

Contact Address of the ethic committee:

399 Wanyuan Road, Minhang District, Shanghai

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 21 6493 1913

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:

复旦大学附属儿科医院

Primary sponsor:

Children's Hospital of Fudan University

研究实施负责(组长)单位地址:

上海市闵行区万源路399号

Primary sponsor's address:

399 Wanyuan Road, Minhang District, Shanghai

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

上海

市(区县):

Country:

China

Province:

Shanghai

City:

单位(医院):

复旦大学附属儿科医院

具体地址:

上海市闵行区万源路399号

Institution
hospital:

Children's Hospital of Fudan University

Address:

399 Wanyuan Road, Minhang District, Shanghai

经费或物资来源:

Source(s) of funding:

None

Target disease:

postoperative pain

Target disease code:

研究类型:

观察性研究

Study type:

Observational study

研究所处阶段:

其它 

Study phase:

N/A

研究设计:

横断面 

Study design:

Cross-sectional 

研究目的:

主要研究目的:两组受试者对PCAP宣教重要性的评价 次要研究目的:两组受试者对PCAP宣教效果、方式、内容及侧重点评价  

Objectives of Study:

Primary outcome: how the anticipants rate the importance of the PCAP education Secondary outcomes: how the anticipants evaluate the form, procedure, the effect, the detail content of the PCAP education

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

患者组: 1,患儿1月≤年龄≤18岁 2,患儿接受择期手术 3,患儿术后使用PCAP 护士组: 所有在使用PCAP外科病房工作的护士

Inclusion criteria

Patient group: 1, the pediatric patients older than 1 month and younger than 18 years 2, the pediatric patients who undergo elective surgery 3, the pediatric patients who use PCAP Nurse group: All the nurses in surgery ward

排除标准:

1,受试者有视觉或听觉障碍 2,患儿有慢性疼痛史 3,受试者拒绝参加研究

Exclusion criteria:

1, with visual or auditory impairments 2, patients with chronic pain history 3, deny to participate

研究实施时间:

Study execute time:

From 2024-05-01 00:00:00 To 2025-05-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2024-07-20 00:00:00 To 2024-10-20 00:00:00  

干预措施:

Interventions:

组别:

病人组

样本量:

240

Group:

Patient group

Sample size:

干预措施:

术后使用病人自控镇痛泵

干预措施代码:

Intervention:

use patient-controlled analgesia pump to control postoperative pain

Intervention code:

组别:

护士组

样本量:

8

Group:

nurse group

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

上海 

市(区县):

 

Country:

China 

Province:

Shanghai 

City:

 

单位(医院):

复旦大学附属儿科医院 

单位级别:

三甲 

Institution
hospital:

Children's Hospital of Fudan University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

PCAP宣教的重要性

指标类型:

主要指标

Outcome:

the importance of the PCAP education

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

两组受试者对PCAP宣教效果的评价

指标类型:

次要指标

Outcome:

Evaluation of PCAP Education Effectiveness by Two Groups of Participants

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:

组织:

Sample Name:

None

Tissue:

人体标本去向

其它  

说明

Fate of sample:

0thers  

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 0 years
最大 Max age 18 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):

不涉及

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

None

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):

ResMan临床试验公共管理平台

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

ResMan clinical Trial Management Public Platform

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:

数据采集和管理由两部分组成:病例记录表(Case Record Form, CRF)和电子采集和管理系统(Electronic Data Capture, EDC)

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

Data acquisition and management consists of two parts: case record form (CRF) and electronic data capture and management system (EDC).

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:

 2024-07-17 16:03:16