格隆溴铵与长托宁在腹腔镜胆囊切除术中的临床观察

注册号:

Registration number:

ChiCTR2500107519 

最近更新日期:

Date of Last Refreshed on:

2025-08-13 11:24:54 

注册时间:

Date of Registration:

2025-08-13 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

格隆溴铵与长托宁在腹腔镜胆囊切除术中的临床观察

Public title:

Clinical observation of glycopyrronium bromide and penehyclidine hydrochloride in laparoscopic cholecystectomy

注册题目简写:

English Acronym:

研究课题的正式科学名称:

格隆溴铵与长托宁在腹腔镜胆囊切除术中的临床观察

Scientific title:

Clinical observation of glycopyrronium bromide and penehyclidine hydrochloride in laparoscopic cholecystectomy

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:

颜慧 

研究负责人:

夏瑞 

Applicant:

Yan Hui 

Study leader:

Rui Xia 

申请注册联系人电话:

Applicant telephone:

+86 15080707084

研究负责人电话:

Study leader's
telephone:

+86 18972161338

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:

895854763@qq.com

研究负责人电子邮件:

Study leader's E-mail:

879560350@qq.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:

湖北省荆州市沙市区江汉北路55号

研究负责人通讯地址:

湖北省荆州市沙市区江汉北路55号

Applicant address:

No. 55, Jianghan North Road, Shaqu City, Jingzhou, Hubei

Study leader's address:

No. 55, Jianghan North Road, Shaqu City, Jingzhou, Hubei

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:

荆州市第一人民医院

Applicant's institution:

The First People’s Hospital of Jingzhou

研究负责人所在单位:

荆州市第一人民医院

Affiliation of the Leader:

The First People’s Hospital of Jingzhou

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:

伦审[YJ202431]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:

荆州市第一人民医院医学伦理委员会

Name of the ethic committee:

Medical Ethics Committee of Jingzhou First People's Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2024-12-31 00:00:00

伦理委员会联系人:

刘彬

Contact Name of the ethic committee:

Liu Bin

伦理委员会联系地址:

湖北省荆州市沙市区江汉北路55号

Contact Address of the ethic committee:

No. 55, Jianghan North Road, Shaqu City, Jingzhou, Hubei

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 716 8113627

伦理委员会联系人邮箱:

Contact email of the ethic committee:

66841709@qq.com

研究实施负责(组长)单位:

荆州市第一人民医院

Primary sponsor:

The First People’s Hospital of Jingzhou

研究实施负责(组长)单位地址:

湖北省荆州市沙市区江汉北路55号

Primary sponsor's address:

No. 55, Jianghan North Road, Shaqu City, Jingzhou, Hubei

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

湖北

市(区县):

Country:

China

Province:

Hubei

City:

单位(医院):

荆州市第一人民医院

具体地址:

湖北省荆州市沙市区江汉北路55号

Institution
hospital:

The First People’s Hospital of Jingzhou

Address:

No. 55, Jianghan North Road, Shaqu City, Jingzhou, Hubei

经费或物资来源:

自筹

Source(s) of funding:

Self-finance

研究疾病:

胆囊结石  

Target disease:

Gallbladder stones

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:

其它 

Study phase:

N/A

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

主要比较格隆溴铵与长托宁对腹腔镜胆囊切除患者围术期的影响,为临床中的合理应用提供参考依据。  

Objectives of Study:

It mainly compares the effects of gronethium bromide and peritonin on the perioperative period of laparoscopic cholecystectomy patients, and provides a reference basis for the rational application in the clinic.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

Inclusion criteria

排除标准:

1.意识不清或有认知功能障碍; 2.对抗胆碱能药物及其组成成分过敏; 3.术前高血压控制不佳者(SBP>160 mmHg 或 DBP >100 mmHg); 4.房室传导阻滞、心动过缓、严重心律失常以及不稳定心绞痛患者; 5.青光眼患者; 6.意识不清或有认知功能障碍者; 7.术后恶心呕吐及晕动史; 8.妊娠或哺乳期; 9.近 3 个月内参加其他药物临床实验; 10.拒绝参加本研究的患者。

Exclusion criteria:

1. Unconsciousness or cognitive impairment; 2. Allergy to anticholinergic drugs and their constituents; 3. Poorly controlled hypertension (SBP > 160 mmHg or DBP >100 mmHg); 4. Patients with atrioventricular block, bradycardia, severe arrhythmia and unstable angina pectoris; 5. Patients with glaucoma; 6. Unconsciousness or cognitive impairment; 7. History of postoperative nausea, vomiting and motion sickness; 8. Pregnancy or lactation; 9. Participated in other drug clinical trials within the past 3 months; 10. Patients who refused to participate in the study.

研究实施时间:

Study execute time:

From 2025-01-01 00:00:00 To 2025-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2025-01-06 00:00:00 To 2025-12-25 00:00:00

干预措施:

Interventions:

组别:

生理盐水组(C)组

样本量:

40

Group:

The control group (group C)

Sample size:

干预措施:

生理盐水

干预措施代码:

Intervention:

Saline (medicine)

Intervention code:

组别:

格隆溴铵组(G组)

样本量:

40

Group:

The glycopyrrolate group(group G)

Sample size:

干预措施:

G组静脉注射格隆溴铵4 μg/kg

干预措施代码:

Intervention:

Group G was injected with 4 μg/kg of glycopyrrolate intravenously,

Intervention code:

组别:

长托宁组(P组)

样本量:

40

Group:

Penehyclidine hydrochloride group (group P)

Sample size:

干预措施:

长托宁

干预措施代码:

Intervention:

Penehyclidine hydrochloride

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

湖北 

市(区县):

 

Country:

China

Province:

Hubei

City:

单位(医院):

荆州市第一人民医院 

单位级别:

三甲 

Institution
hospital:

The First People’s Hospital of Jingzhou

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

术后24h 恶心呕吐的发生率

指标类型:

主要指标

Outcome:

Incidence of nausea and vomiting 24h after surgery

Type:

Primary indicator

测量时间点:

术后24h

测量方法:

随访

Measure time point of outcome:

24h after surgery

Measure method:

Follow up

指标中文名:

HR和MAP

指标类型:

次要指标

Outcome:

HR and MAP

Type:

Secondary indicator

测量时间点:

给药前、给药后5 min、给药后10 min、气管插管后1 min、切皮即刻、气腹开始后2 min、游离胆囊时、气管拔管后1 min

测量方法:

观察

Measure time point of outcome:

Before , 5 min after , 10 min after , 1 min after tracheal intubation , at the moment of skin incis

Measure method:

Heed

指标中文名:

口腔腺体分泌量、PACU的停留时间

指标类型:

次要指标

Outcome:

Oral glandular secretion, length of stay in the PACU

Type:

Secondary indicator

测量时间点:

术后

测量方法:

观察

Measure time point of outcome:

Postoperative

Measure method:

Heed

指标中文名:

口干(口苦)、谵妄、尿潴留和首次排气时间

指标类型:

次要指标

Outcome:

Dry mouth (xerostomia), delirium, urinary retention, and time to first venting

Type:

Secondary indicator

测量时间点:

术后

测量方法:

随访

Measure time point of outcome:

Postoperative

Measure method:

Follow up

指标中文名:

低血压、心动过缓

指标类型:

次要指标

Outcome:

Hypotension, bradycardia

Type:

Secondary indicator

测量时间点:

术中

测量方法:

观察

Measure time point of outcome:

Intraoperative

Measure method:

Heed

指标中文名:

术后1 h恶心呕吐发生率

指标类型:

次要指标

Outcome:

Incidence of nausea and vomiting at 1 h postoperatively.

Type:

Secondary indicator

测量时间点:

术后

测量方法:

观察

Measure time point of outcome:

postoperative

Measure method:

Heed

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

组织:

Sample Name:

N/A

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:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 64 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):

计算机生成随机序列方法

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

Computer Generated Random Sequence Methods

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

Blinding:

Double blind

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):

qq邮箱895854763@qq.com,试验结束后

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

QQ email 895854763@qq.com, after the trial concludes

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:

Case Record Form

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2025-08-13 11:24:46