ChiCTR2500114045 版本V1.0 版本创建时间2025/12/05 17:20:52 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:

ChiCTR2500114045 

最近更新日期:

Date of Last Refreshed on:

2025-12-05 17:14:52 

注册时间:

Date of Registration:

2025-12-05 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

比较瑞马唑仑、丙泊酚、七氟烷对行口内手术患者苏醒期躁动的影响:一项多中心、随机、对照试验

Public title:

Effects of Remimazolam, Propofol, and Sevoflurane on Emergence Agitation in Patients Undergoing Oral Surgery: A Multicenter, Randomized, Controlled Trial

注册题目简写:

English Acronym:

研究课题的正式科学名称:

比较瑞马唑仑、丙泊酚、七氟烷对行口内手术患者苏醒期躁动的影响:一项多中心、随机、对照试验

Scientific title:

Effects of Remimazolam, Propofol, and Sevoflurane on Emergence Agitation in Patients Undergoing Oral Surgery: A Multicenter, Randomized, Controlled Trial

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:

彭科 

研究负责人:

彭科 

Applicant:

Peng Ke 

Study leader:

KePeng 

申请注册联系人电话:

Applicant telephone:

+86 512 6797 6629

研究负责人电话:

Study leader's telephone:

+86 512 6778 0156

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:

pengke0422@163.com

研究负责人电子邮件:

Study leader's E-mail:

pengke0422@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:

江苏省苏州市姑苏区平海路899号

研究负责人通讯地址:

平海路899号

Applicant address:

899 Pinghai Road, Gusu, Suzhou, Jiangsu

Study leader's address:

Pinghai Road no.899

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:

苏州大学附属第一医院麻醉科

Applicant's institution:

Department of Anesthesiology, First Affiliated Hospital of Soochow University

研究负责人所在单位:

苏州大学附属第一医院

Affiliation of the Leader:

The First Affiliated Hospital of Soochow 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:

(2025)伦审批第900 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:

苏州大学附属第一医院医学伦理委员会

Name of the ethic committee:

First Affiliated Hospital of Soochow University Medical Ethics Committee

伦理委员会批准日期:

Date of approved by ethic committee:

2025-09-30 00:00:00

伦理委员会联系人:

陆周琳

Contact Name of the ethic committee:

Lu ZhouLin

伦理委员会联系地址:

平海路899号

Contact Address of the ethic committee:

Pinghai Road no.899

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 512 6797 2861

伦理委员会联系人邮箱:

Contact email of the ethic committee:

809580153@qq.com

研究实施负责(组长)单位:

苏州大学附属第一医院

Primary sponsor:

The First Affiliated Hospital of Soochow University

研究实施负责(组长)单位地址:

平海路899号

Primary sponsor's address:

Pinghai Road no.899

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

江苏省

市(区县):

Country:

China

Province:

Jiangsu

City:

单位(医院):

苏州大学附属第一医院

具体地址:

平海路899号

Institution
hospital:

The First Affiliated Hospital of Soochow University

Address:

Pinghai Road no.899

经费或物资来源:

自选课题(自筹)

Source(s) of funding:

Self-funded project

Target disease:

Emergence agitation (EA) is a common complication following general anesthesia, characterized by a state of confusion, disorientation, restlessness, crying, or purposeless movements during the recovery period.

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

其它 

Study phase:

N/A

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

在接受口内手术患者中比较瑞马唑仑、丙泊酚、七氟烷麻醉对于EA发生率的影响,为优化该类手术患者的麻醉方案提供高级别循证依据。  

Objectives of Study:

This study compares the effects of remimazolam, propofol, and sevoflurane anesthesia on the incidence of emergence agitation (EA) in patients undergoing oral surgery, aiming to provide high-level evidence for optimizing anesthesia protocols in this patient population.

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.年龄 18~70岁;
2.ASA分级 I~III级;
3.接受择期经鼻气管插管全麻下行口内手术的患者;

Inclusion criteria

1.Aged 18 to 70 years;
2.ASA physical status I to III;
3.Scheduled for elective oral surgery under general anesthesia with nasotracheal intubation;

排除标准:

1.体重指数(BMI)>35 kg/m2;
2.术前1个月内接受过全身麻醉或镇静治疗;
3.缺血性心脏病、NYHA ≥ III级、3个月内急性冠脉综合征或卒中;
4.神经精神系统疾病(精神分裂症、癫痫、帕金森症、阿尔兹海默症);
5.严重肝功能障碍(Child-Pugh C);
6.肾功能不全(eGFR < 30 mL/min/1.73 m2或需透析);
7.未控制的糖尿病(空腹血糖 > 11 mmol/L);
8.颅底骨折;
9.既往鼻腔手术史、严重鼻中隔偏曲、复发性鼻出血史;

Exclusion criteria:

1.Body mass index (BMI) >35 kg/m^2; 2.General anesthesia or sedation within one month prior to surgery; 3.Ischemic heart disease, NYHA >= class III, acute coronary syndrome or stroke within 3 months; 4.Pre-existing neuropsychiatric disorders (e.g., history of schizophrenia, epilepsy, Parkinson's disease, or Alzheimer's disease); 5.Hepatic dysfunction (Child-Pugh C); 6.Renal insufficiency (eGFR < 30 mL/min/1.73 m^2 or requiring dialysis); 7.Uncontrolled diabetes (fasting blood glucose > 11 mmol/L); 8.Skull base fracture; 9.Previous nasal surgery, severe deviated nasal septum, or recurrent epistaxis;

研究实施时间:

Study execute time:

From 2025-12-15 00:00:00 To 2026-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2025-12-15 00:00:00 To 2026-12-31 00:00:00  

干预措施:

Interventions:

组别:

瑞马唑仑组

样本量:

130

Group:

Remimazolam group

Sample size:

干预措施:

瑞马唑仑全身麻醉

干预措施代码:

Intervention:

General anesthesia with remimazolam

Intervention code:

组别:

丙泊酚组

样本量:

130

Group:

Propofol group

Sample size:

干预措施:

丙泊酚全身麻醉

干预措施代码:

Intervention:

General anesthesia with propofol

Intervention code:

组别:

七氟烷组

样本量:

130

Group:

Sevoflurane group

Sample size:

干预措施:

七氟烷全身麻醉

干预措施代码:

Intervention:

General anesthesia with sevoflurane

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

江苏省 

市(区县):

 

Country:

China 

Province:

Jiangsu 

City:

 

单位(医院):

苏州大学附属第一医院 

单位级别:

三级甲等 

Institution
hospital:

The First Affiliated Hospital of Soochow University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

苏醒期躁动发生率

指标类型:

主要指标

Outcome:

The incidence of emergence agitation

Type:

Primary indicator

测量时间点:

从停止麻醉药物(瑞马唑仑、丙泊酚、七氟烷)到拔除气管导管5分钟后

测量方法:

最大的Riker镇静-躁动量表(SAS)评分 ≥ 5

Measure time point of outcome:

From the discontinuation of anesthetic agents until 5 min after extubation

Measure method:

Maximum Riker Sedation Agitation Scale (SAS) score >= 5

指标中文名:

术后24h恢复质量

指标类型:

次要指标

Outcome:

Quality of recovery at 24 hours postoperatively

Type:

Secondary indicator

测量时间点:

术后24小时

测量方法:

QoR-15恢复质量评分量表

Measure time point of outcome:

24 hours postoperatively

Measure method:

QoR-15 scale

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

组织:

Sample Name:

NA

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 18 years
最大 Max age 70 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):

由一位不参与招募或研究的统计学家,基于网络工具(www.sealedenvelope.com)进行随机分配,比例为1:1:1,区组大小为3和6,并按研究中心分层

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

Randomization will be conducted by a statistician not involved in recruitment or other parts of the study, using a web-based tool (www.sealedenvelope.com) with a 1:1:1 ratio and block sizes of 3 and 6, and stratified by study center.

是否公开试验完成后的统计结果:

Calculated Results after the Study Completed public access:

不公开/Private

盲法:

双盲(结局评估者与受试者设盲)

Blinding:

Double-blind (blinding of both outcome assessors and participants)

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):

数据可根据合理请求向通讯作者索取。

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

Data are available upon reasonable request from the corresponding author.

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:

病历记录表,电子采集和管理系统

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

CRF and Electronic Collection and Management System

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2025-12-05 17:14:52