ChiCTR2200056551 版本V1.6 版本创建时间2024/10/06 22:01:21 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:

ChiCTR2200056551 

最近更新日期:

Date of Last Refreshed on:

2023-08-29 17:44:00 

注册时间:

Date of Registration:

2022-02-07 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

零阿片术后自控镇痛策略在胸科腔镜手术的应用

Public title:

Application of opioid free-patient control analgesia in thoracic endoscopic surgery

注册题目简写:

English Acronym:

研究课题的正式科学名称:

零阿片术后自控镇痛策略在胸科腔镜手术的应用

Scientific title:

Application of opioid free-patient control analgesia in thoracic endoscopic surgery

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:

李汶谦 

研究负责人:

李晓霞 

Applicant:

Li Wenqian 

Study leader:

Li Xiaoxia 

申请注册联系人电话:

Applicant telephone:

+86 13167947336

研究负责人电话:

Study leader's
telephone:

+86 13368380465

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:

2021120456@stu.cqmu.edu.cn

研究负责人电子邮件:

Study leader's E-mail:

300465@hospital.cqmu.edu.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:

重庆市渝中区临江路76号重庆医科大学附属第二医院麻醉科

研究负责人通讯地址:

重庆市渝中区临江路76号重庆医科大学附属第二医院麻醉科

Applicant address:

76 Linjiang Road, Yuzhong District, Chongqing

Study leader's address:

76 Linjiang Road, Yuzhong District, Chongqing

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:

重庆医科大学附属第二医院麻醉科

Applicant's institution:

The Second Affiliated Hospital of Chongqing Medical University

研究负责人所在单位:

重庆医科大学附属第二医院麻醉科

Affiliation of the Leader:

The Second Affiliated Hospital of Chongqing Medical University

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:

2022年科伦审第(9-1)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:

重庆医科大学附属第二医院伦理委员会

Name of the ethic committee:

Ethics Committee of the Second Affiliated Hospital of Chongqing Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2022-08-18 00:00:00

伦理委员会联系人:

敖俊

Contact Name of the ethic committee:

Ao Jun

伦理委员会联系地址:

重庆市渝中区临江路76号重庆医科大学附属第二医院

Contact Address of the ethic committee:

76 Linjiang Road, Yuzhong District, Chongqing

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 23 63693472

伦理委员会联系人邮箱:

Contact email of the ethic committee:

300465@hospital.cqmu.edu.cn

研究实施负责(组长)单位:

重庆医科大学附属第二医院麻醉科

Primary sponsor:

The Second Affiliated Hospital of Chongqing Medical University

研究实施负责(组长)单位地址:

重庆市渝中区临江路76号重庆医科大学附属第二医院麻醉科

Primary sponsor's address:

76 Linjiang Road, Yuzhong District, Chongqing

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

重庆

市(区县):

Country:

China

Province:

Chongqing

City:

单位(医院):

重庆医科大学附属第二医院

具体地址:

渝中区临江路76号

Institution
hospital:

The Second Affiliated Hospital of Chongqing Medical University

Address:

76 Linjiang Road, Yuzhong District

经费或物资来源:

Source(s) of funding:

None

研究疾病:

N/A  

Target disease:

N/A

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:

随机平行对照 

Study design:

Parallel 

研究目的:

观察零阿片镇痛策略(艾司氯胺酮复合右美托咪定)在胸科手术后静脉自控镇痛(PCIA)的可行性、镇痛效果及恶心呕吐发生率。  

Objectives of Study:

To observe the feasibility, analgesic effect and incidence of nausea and vomiting of free-opioid analgesia strategy (esketamine combined with dexmedetomidine) in patient-controlled intravenous analgesia (PCIA) after thoracic surgery.

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.美国麻醉医师协会 (ASA)分级 I-III 级;
2.年龄 19~65 岁,能够熟练应用 PCA 泵;
3.理解并充分配合使用术后各项评分工具。

Inclusion criteria

1. American Society of Anesthesiologists (ASA) Class I-III;
2. Aged 19-65 years, skilled in PCA pump application;
3. Understand and fully cooperate with postoperative scoring tools.

排除标准:

1.体重指数(body mass index,BMI)>30kg/m^2;
2.近 6 个月内出现心绞痛或心肌梗死病史;
3.控制不佳的或未经治疗的高血压患者(静息收缩压/舒张压>180/100mmHg);
4.未经治疗或治疗不足的甲亢患者;
5.肝肾功能不全患者;
6.神经精神疾患者;
7.长期酗酒者;
8.长期使用镇静催眠镇痛药物;
9.心率<50 次/min 或有 III 度房室传导阻滞;
10.已知对试验药物如右美托咪定或/和艾司氯胺酮过敏;
11.术中更改手术方式者;
12.围手术期患者资料丢失。

Exclusion criteria:

1. Body mass index (BMI)>30kg/m^2;
2. A history of angina pectoris or myocardial infarction in the past 6 months;
3. Patients with poorly controlled or untreated hypertension (resting systolic/diastolic blood pressure >180/100 MMHG);
4. Untreated or undertreated hyperthyroidism;
5. Patients with liver and kidney dysfunction;
6. Patients with neuropsychiatric disorders;
7. Chronic alcoholics;
8. Long-term use of sedative, hypnotic and analgesic drugs;
9. Heart rate < 50 beats/min or degree III atrioventricular block;
10. Known allergy to test drugs such as dexmedetomidine or/and esketamine;
11. Change the operation method during the operation;
12. Loss of perioperative patient data.

研究实施时间:

Study execute time:

From 2021-09-01 00:00:00 To 2023-07-11 00:00:00  

征募观察对象时间:

Recruiting time:

From 2022-02-01 00:00:00 To 2023-03-31 00:00:00

干预措施:

Interventions:

组别:

1组

样本量:

30

Group:

Group 1

Sample size:

干预措施:

艾司氯胺酮+右美托咪定+托烷司琼

干预措施代码:

Intervention:

Esketamine, dexmedetomidine and tropisetron

Intervention code:

组别:

2组

样本量:

30

Group:

Group 2

Sample size:

干预措施:

舒芬太尼+右美托咪定+托烷司琼

干预措施代码:

Intervention:

Sufentanil, dexmedetomidine and tropisetron

Intervention code:

组别:

3组

样本量:

30

Group:

Group 3

Sample size:

干预措施:

右美托咪定+曲马多+托烷司琼

干预措施代码:

Intervention:

Dexmedetomidine, tramadol and tropisetron

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

重庆 

市(区县):

 

Country:

China

Province:

Chongqing

City:

单位(医院):

重庆医科大学附属第二医院 

单位级别:

三级甲等 

Institution
hospital:

The Second Affiliated Hospital of Chongqing Medical University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

恶心呕吐

指标类型:

主要指标

Outcome:

Nausea and vomiting

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

视觉模拟评分法疼痛评分

指标类型:

次要指标

Outcome:

Visual analogue scale pain 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:

Ramsay镇静评分

指标类型:

次要指标

Outcome:

Ramsay sedation 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:

BCS舒适度评分

指标类型:

次要指标

Outcome:

BCS comfort 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:

平均动脉压

指标类型:

次要指标

Outcome:

Mean arterial pressure

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

心率

指标类型:

次要指标

Outcome:

Heart rate

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

呼吸频率

指标类型:

次要指标

Outcome:

Breathing rate

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血氧饱和度

指标类型:

次要指标

Outcome:

SpO2

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:

Null

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 19 years
最大 Max age 65 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):

计算机产生随机数字表

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

Computer generated random number table

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:

双盲(细节未说明)

Blinding:

Double blind (details not specified)

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

否No

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):

无 (请阅读网站首页注册指南共享原始数据的方式内容)

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

None

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:

未说明

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

Not stated

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2022-02-07 12:23:06