纳美芬对术后镇痛的影响观察,一项多中心前瞻性随机双盲对照试验

注册号:

Registration number:

ChiCTR2000032472 

最近更新日期:

Date of Last Refreshed on:

2020-04-29 23:26:11 

注册时间:

Date of Registration:

2020-04-29 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

纳美芬对术后镇痛的影响观察,一项多中心前瞻性随机双盲对照试验

Public title:

Effects of nalmefene on postoperative analgesia, a multicenter, prospective, randomized, double-blinded controlled trial

注册题目简写:

English Acronym:

研究课题的正式科学名称:

纳美芬对术后镇痛的影响观察,一项多中心前瞻性随机双盲对照试验

Scientific title:

Effects of nalmefene on postoperative analgesia, a multicenter, prospective, randomized, double-blinded 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:

殷德坤 

研究负责人:

殷德坤 

Applicant:

Dekun Yin 

Study leader:

Dekun Yin 

申请注册联系人电话:

Applicant telephone:

+86 15805110243

研究负责人电话:

Study leader's
telephone:

+86 15805110243

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:

153761717@qq.com

研究负责人电子邮件:

Study leader's E-mail:

kundymedical@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:

江苏省盐城阜宁县阜城大街111号

研究负责人通讯地址:

江苏省盐城阜宁县阜城大街111号

Applicant address:

111 Fucheng Street, Funing County, Yancheng, Jiangsu, China

Study leader's address:

111 Fucheng Street, Funing County, Yancheng, Jiangsu, China

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:

江苏省阜宁县人民医院

Applicant's institution:

Funing People's Hospital of Jiangsu Province

研究负责人所在单位:

江苏省阜宁县人民医院

Affiliation of the Leader:

Funing People's Hospital of Jiangsu Province

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:

2020031002

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:

阜宁县人民医院临床试验伦理委员会

Name of the ethic committee:

Clinical Trials Ethics Committee of Funing People's Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2020-03-10 00:00:00

伦理委员会联系人:

嵇亚军

Contact Name of the ethic committee:

Yajun Ji

伦理委员会联系地址:

江苏省盐城阜宁县阜城大街111号

Contact Address of the ethic committee:

111 Fucheng Street, Funing County, Yancheng, Jiangsu, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

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:

江苏省阜宁县人民医院

Primary sponsor:

Funing People's Hospital of Jiangsu Province

研究实施负责(组长)单位地址:

江苏省阜宁县阜城大街111号

Primary sponsor's address:

111 Fucheng Street, Funing County, Yancheng, Jiangsu, China

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

市(区县):

盐城

Country:

China

Province:

Jiangsu

City:

Yancheng

单位(医院):

阜宁县人民医院

具体地址:

阜宁县阜城大街111号

Institution
hospital:

Funing People's Hospital of Jiangsu Province

Address:

111 Fucheng Street, Funing County

经费或物资来源:

阜宁县人民医院科研基金

Source(s) of funding:

Research Fund of Funing People's Hospital of Jiangsu Province

研究疾病:

单发性上肢/下肢/锁骨骨折术后镇痛观察  

Target disease:

Observation on postoperative analgesia of single upper limb fracture/ lower extremity fracture / clavicle fracture

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:

上市后药物 

Study phase:

4

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

观察少量纳美芬的同时使用,对术后镇痛药的镇痛效果、副作用的影响。  

Objectives of Study:

To observe the analgesic effect and side effects of postoperative analgesics after a small amount of nalmefene being used at the same time.

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. 孕期、哺乳期妇女;
2. 有长期疼痛性疾病史;
3. 阿片类药物或其拮抗剂过敏史;
4. 药物或酒精依赖史
5. 合并严重心肺功能及肝肾等器官功能障碍者;
6. 严重鼾症、过于肥胖者(BMI>30kg/㎡);
7. 有消化系统疾病史者;
8. 高血压、糖尿病、精神障碍、智力不正常者。

Exclusion criteria:

1. Pregnant and lactating women;
2. Patients with a long history of painful diseases;
3. Patients with allergic history of opioids or their antagonists;
4. Patients with a history of drug or alcohol dependence;
5. Patients with severe cardiopulmonary function, liver and kidney dysfunction;
6. Patients with severe snoring and obesity (BMI > 30 kg / m2);
7. Patients with history of digestive system diseases;
8. Patients with high blood pressure, diabetes, mental disorders and mental disorders.

研究实施时间:

Study execute time:

From 2020-05-01 00:00:00 To 2022-05-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2020-05-01 00:00:00 To 2022-05-01 00:00:00

干预措施:

Interventions:

组别:

地佐辛C组

样本量:

60

Group:

Dezocine C group

Sample size:

干预措施:

安慰剂

干预措施代码:

Intervention:

placebo

Intervention code:

组别:

地佐辛N组

样本量:

60

Group:

dezocine N group

Sample size:

干预措施:

纳美芬

干预措施代码:

Intervention:

nalmefene

Intervention code:

组别:

芬太尼C组

样本量:

60

Group:

fentanyl C group

Sample size:

干预措施:

安慰剂

干预措施代码:

Intervention:

placebo

Intervention code:

组别:

芬太尼N组

样本量:

60

Group:

fentanyl N group

Sample size:

干预措施:

纳美芬

干预措施代码:

Intervention:

nalmefene

Intervention code:

组别:

舒芬太尼C组

样本量:

60

Group:

sufentanil C group

Sample size:

干预措施:

安慰剂

干预措施代码:

Intervention:

placebo

Intervention code:

组别:

舒芬太尼N组

样本量:

60

Group:

sufentanil N group

Sample size:

干预措施:

纳美芬

干预措施代码:

Intervention:

nalmefene

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

江苏 

市(区县):

盐城 

Country:

China

Province:

Jiangsu

City:

Yancheng

单位(医院):

阜宁县人民医院 

单位级别:

二甲 

Institution
hospital:

Funing People's Hospital of Jiangsu Province

Level of the institution:

Secondary A

国家:

中国

省(直辖市):

江苏 

市(区县):

南通 

Country:

China

Province:

Jiangsu

City:

Nantong

单位(医院):

南通大学附属医院 

单位级别:

三甲 

Institution
hospital:

The Affiliated Hospital of Nantong University

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

上海 

市(区县):

徐汇区 

Country:

China

Province:

Shanghai

City:

Xuhui District

单位(医院):

上海第六人民医院 

单位级别:

三甲 

Institution
hospital:

The Sixth People's Hospital of Shanghai

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

视觉模拟评分

指标类型:

主要指标

Outcome:

Visual Analogue Scale/Score

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

患者的基本信息

指标类型:

次要指标

Outcome:

Basic information of patients

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

术中情况

指标类型:

次要指标

Outcome:

Intraoperative condition

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

术前情况

指标类型:

主要指标

Outcome:

Preoperative condition

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

生命体征

指标类型:

主要指标

Outcome:

Vital signs

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

镇痛药副作用指标

指标类型:

主要指标

Outcome:

Outcome of side effects of analgesics

Type:

Primary 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:

主要指标

Outcome:

Ramsay Sedation score

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

OAA/S 镇静评级标准

指标类型:

主要指标

Outcome:

OAA/S sedation rating standard

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

自控镇痛泵使用情况

指标类型:

主要指标

Outcome:

application of self-control analgesia pump

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

患者睡眠质量

指标类型:

主要指标

Outcome:

Sleep quality of patients

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

预测模型参数

指标类型:

主要指标

Outcome:

Forecast model parameters

Type:

Primary 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:

nil

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 years
最大 Max age 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):

计算机产生的随机序列。

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

Computed randomized table.

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):

2022年9月后,可向研究负责人发送电子邮件索要

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

After September 2022, an email request can be sent to the study leader.

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, CRF

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2020-04-29 17:37:26