ChiCTR2400087856 版本V1.1 版本创建时间2024/08/06 09:47:32 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:

ChiCTR2400087856 

最近更新日期:

Date of Last Refreshed on:

2024-08-06 09:47:25 

注册时间:

Date of Registration:

2024-08-06 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

儿科患者喉罩气道尺寸选择:一种基于身高的筛选方法

Public title:

Height-based method for laryngeal mask airway size selection in pediatric patients

注册题目简写:

English Acronym:

研究课题的正式科学名称:

儿科患者喉罩气道尺寸选择:一种基于身高的筛选方法

Scientific title:

Height-based method for laryngeal mask airway size selection in pediatric patients

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:

全玲来 

研究负责人:

全玲来 

Applicant:

Quan Linglai  

Study leader:

Quan Linglai  

申请注册联系人电话:

Applicant telephone:

+86 177 0651 1929

研究负责人电话:

Study leader's
telephone:

+86 177 0651 1929

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:

quanlinglai@eye.ac.cn

研究负责人电子邮件:

Study leader's E-mail:

quanlinglai@eye.ac.cn

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:

浙江省杭州市上城区凤起东路618号

研究负责人通讯地址:

浙江省杭州市上城区凤起东路618号

Applicant address:

618 Fengqi East Road, Shangcheng District, Hangzhou, Zhejiang

Study leader's address:

618 Fengqi East Road, Shangcheng District, Hangzhou, Zhejiang

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:

温州医科大学附属眼视光医院杭州院区

Applicant's institution:

Optometry Hospital Affiliated to Wenzhou Medical University, Hangzhou District

研究负责人所在单位:

温州医科大学附属眼视光医院杭州院区

Affiliation of the Leader:

Optometry Hospital Affiliated to Wenzhou Medical University, Hangzhou District

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:

温医大眼视光(杭)伦审2024研第003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:

温州医科大学附属眼视光医院杭州院区伦理委员会

Name of the ethic committee:

Ethics Committee of Hangzhou District, Optometry Hospital Affiliated to Wenzhou Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2024-03-18 00:00:00

伦理委员会联系人:

陈红霞

Contact Name of the ethic committee:

Chen Hongxia

伦理委员会联系地址:

浙江省杭州市上城区凤起东路618号

Contact Address of the ethic committee:

618 Fengqi East Road, Shangcheng District, Hangzhou, Zhejiang

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 571 8672 6050

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:

温州医科大学附属眼视光医院杭州院区

Primary sponsor:

Optometry Hospital Affiliated to Wenzhou Medical University, Hangzhou District

研究实施负责(组长)单位地址:

浙江省杭州市上城区凤起东路618号

Primary sponsor's address:

618 Fengqi East Road, Shangcheng District, Hangzhou, Zhejiang

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

浙江省

市(区县):

Country:

China

Province:

Zhejiang

City:

单位(医院):

温州医科大学附属眼视光医院杭州院区

具体地址:

浙江省杭州市上城区凤起东路618号

Institution
hospital:

Optometry Hospital Affiliated to Wenzhou Medical University, Hangzhou District

Address:

618 Fengqi East Road, Shangcheng District, Hangzhou, Zhejiang

经费或物资来源:

自筹

Source(s) of funding:

Self-raised

研究疾病:

小儿麻醉  

Target disease:

paediatric anaesthesia

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:

探索性研究/预试验 

Study phase:

0

研究设计:

队列研究 

Study design:

Cohort study 

研究目的:

评估在推荐的口咽漏压下,身高对喉罩选择的影响,以指导小儿喉罩的最佳选择型号。  

Objectives of Study:

To assess the effect of height on oropharyngeal leak pressure (OLP) in children at the recommended intracuff pressure.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

接受眼科全身麻醉,年龄在2 岁至 7岁区间、ASA I -II 级的患者入组。

Inclusion criteria

Patients between 2 and 7 years of age,underwent elective ophthalmic surgery and had an American Society of Anesthesiologists physical status rating of I or II were enrolled.

排除标准:

①患有心脏病、呼吸系统疾病或精神障碍的患者。②有误吸风险或上呼吸道异常的患者。

Exclusion criteria:

① Patients with heart disease, respiratory disease or mental disorder. ② Patients at risk of aspiration or abnormal upper respiratory tract.

研究实施时间:

Study execute time:

From 2024-08-01 00:00:00 To 2024-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2024-08-06 00:00:00 To 2024-12-31 00:00:00

干预措施:

Interventions:

组别:

实验组

样本量:

54

Group:

Test group

Sample size:

干预措施:

按照标准化表格,以患儿身高所在人群P50的体重(标准体重)选择喉罩。

干预措施代码:

Intervention:

According to the standardized form, the laryngeal mask was selected according to the weight of P50 (standard weight) with the height of the child.

Intervention code:

组别:

对照组

样本量:

54

Group:

Control group

Sample size:

干预措施:

根据实际体重选择喉罩。

干预措施代码:

Intervention:

The laryngeal mask was selected according to the actual weight.

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

浙江省 

市(区县):

 

Country:

China

Province:

Zhengjiang

City:

单位(医院):

温州医科大学附属眼视光医院杭州院区 

单位级别:

三甲 

Institution
hospital:

Optometry Hospital Affiliated to Wenzhou Medical University, Hangzhou District

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

口咽漏压

指标类型:

主要指标

Outcome:

Oropharyngeal leak pressure

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

通气质量

指标类型:

次要指标

Outcome:

Quality of ventilation

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

纤维支气管镜分级

指标类型:

次要指标

Outcome:

Fibreoptic bronchoscope position grade

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

插入的难易程度

指标类型:

次要指标

Outcome:

Ease of insertion

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

吸气峰值压力

指标类型:

次要指标

Outcome:

Peak inspiratory pressure

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

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 2 years
最大 Max age 7 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):

研究者根据随机数字表法分组

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

Random number table method

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):

试验完成后可以给主要负责人发邮件索取原始数据

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

After the test is completed, you can email the main person in charge to request the original data

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:

数据采集后记录在CRF表格上

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

Data is recorded on the 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:

 2024-08-06 09:46:58