研究者撤销 剖宫产术中应用小剂量艾司氯胺酮镇痛对产后抑郁的影响

注册号:

Registration number:

ChiCTR2000030698 

最近更新日期:

Date of Last Refreshed on:

2023-06-08 11:13:38 

注册时间:

Date of Registration:

2020-03-10 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

研究者撤销 剖宫产术中应用小剂量艾司氯胺酮镇痛对产后抑郁的影响

Public title:

Canceled by the investigator. Low-dose esketamine for cesarean section effects on postpartum depression

注册题目简写:

English Acronym:

研究课题的正式科学名称:

剖宫产术中应用小剂量艾司氯胺酮镇痛 对产后抑郁的影响

Scientific title:

Low-dose esketamine for cesarean section effects on postpartum depression

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:

薛杭 

研究负责人:

赵平 

Applicant:

Hang Xue 

Study leader:

Ping Zhao 

申请注册联系人电话:

Applicant telephone:

+86 18940256471

研究负责人电话:

Study leader's
telephone:

+86 18940258971

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:

xuehang0407@163.com

研究负责人电子邮件:

Study leader's E-mail:

zhaop@sj-hospital.org

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:

辽宁省沈阳市和平区三好街36号

研究负责人通讯地址:

辽宁省沈阳市和平区三好街36号

Applicant address:

36 Sanhao Street, Heping District, Shenyang, Liaoning, China

Study leader's address:

36 Sanhao Street, Heping District, Shenyang, Liaoning, China

申请注册联系人邮政编码:

Applicant postcode:

110004

研究负责人邮政编码:

Study leader's postcode:

申请人所在单位:

中国医科大学附属盛京医院麻醉科

Applicant's institution:

Department of Anesthesiology, Shengjing Hospital, China Medical University

研究负责人所在单位:

中国医科大学附属盛京医院

Affiliation of the Leader:

Department of Anesthesiology, Shengjing Hospital, China Medical University

是否获伦理委员会批准:

Approved by ethic committee:

No

伦理委员会批件文号:

Approved No. of ethic committee:

伦理委员会批件附件:

Approved file of Ethical Committee:

批准本研究的伦理委员会名称:

Name of the ethic committee:

伦理委员会批准日期:

Date of approved by ethic committee:

伦理委员会联系人:

Contact Name of the ethic committee:

伦理委员会联系地址:

Contact Address of the ethic committee:

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:

中国医科大学附属盛京医院

Primary sponsor:

Department of Anesthesiology, Shengjing Hospital, China Medical University

研究实施负责(组长)单位地址:

辽宁省沈阳市和平区三好街36号

Primary sponsor's address:

36 Sanhao Street, Heping District, Shenyang, Liaoning, 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):

辽宁省

市(区县):

沈阳

Country:

China

Province:

Liaoning

City:

Shenyang

单位(医院):

中国医科大学附属盛京医院麻醉科

具体地址:

和平区三好街36号

Institution
hospital:

Department of Anesthesiology, Shengjing Hospital, China Medical University

Address:

36 Sanhao Street, Heping District

经费或物资来源:

国家自然基金面上项目(No.81671311 No.81870838),辽宁省重点研发计划指导计划项目(No.2018225004),盛京自由研究者(No. 201708)

Source(s) of funding:

This work was supported by the National Nature Science Foundation of China (No. 81671311, No.81870838), the Key Research and Development Program of Liaoning Province (No.2018225004), and the Outstandi

研究疾病:

产后抑郁  

Target disease:

Postpartum depression

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:

研究剖宫产术中应用小剂量氯胺酮镇痛对产后抑郁发生率的影响。  

Objectives of Study:

To study the effect of low-dose ketamine analgesia on the incidence of postpartum depression during cesarean section.

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.产妇有抑郁史; 2.产妇经历过家庭暴力; 3.产妇存在严重的产科并发症或严重基础疾病; 4.新生儿存在严重的遗传疾病或先天性疾病; 5.多胎妊娠; 6.产妇体重<50公斤或>100公斤,身高<150cm或>180cm。

Exclusion criteria:

1. The mother has a history of depression; 2.The mother has experienced domestic violence; 3. The mother has severe obstetric complications or serious underlying diseases; 4. The newborn has a severe genetic or congenital disease; 5. Multiple pregnancy; 6. Weight < 50 kg or > 100 kg, height < 150cm or > 180cm.

研究实施时间:

Study execute time:

From 2020-04-01 00:00:00 To 2021-06-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2020-04-01 00:00:00 To 2021-06-01 00:00:00

干预措施:

Interventions:

组别:

安慰剂

样本量:

180

Group:

control group

Sample size:

干预措施:

注射安慰剂0.9%生理盐水溶液5ml

干预措施代码:

Intervention:

5ml of 0.9% physiological saline solution

Intervention code:

组别:

氯胺酮组

样本量:

180

Group:

ketamine group

Sample size:

干预措施:

静脉内注射艾司氯胺酮0.25mg/kg,使用0.9%生理盐水溶为5ml无色透明溶液

干预措施代码:

Intervention:

Intravenous injection of esketamine 0.25mg / kg, dissolved in 5ml colorless transparent solution with 0.9% physiological saline.

Intervention code:

组别:

诺扬组

样本量:

180

Group:

Butorphanol Tartrate group

Sample size:

干预措施:

常规注射诺扬0.5mg,使用0.9%生理盐水溶为5ml

干预措施代码:

Intervention:

Conventional injection of Noyang 0.5mg, dissolved in 0.9% saline 5ml.

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

辽宁 

市(区县):

沈阳 

Country:

China

Province:

Liaoning

City:

Shenyang

单位(医院):

中国医科大学附属盛京医院麻醉科 

单位级别:

三甲 

Institution
hospital:

Department of Anesthesiology, Shengjing Hospital, China Medical University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

产前基本信息

指标类型:

次要指标

Outcome:

basic information

Type:

Secondary indicator

测量时间点:

测量方法:

年龄、BMI、职业、文化程度、与伴侣关系等

Measure time point of outcome:

Measure method:

指标中文名:

术中指标

指标类型:

次要指标

Outcome:

intraoperative

Type:

Secondary indicator

测量时间点:

测量方法:

产时记录首次镇痛请求的时间、低血压和麻黄碱的需求、心动过缓和低血氧症等不良反应的发生率,记录产后前24小时的镇痛要求

Measure time point of outcome:

Measure method:

指标中文名:

术后指标

指标类型:

次要指标

Outcome:

postoperative

Type:

Secondary indicator

测量时间点:

测量方法:

产后第二天,使用视觉疼痛量表评分评价产妇的刀口痛、宫缩痛,记录睡眠质量与时长,记录产妇服用去痛片情况,记录恶心、呕吐、头晕头迷、噩梦、幻视等副作用的发生情况。

Measure time point of outcome:

Measure method:

指标中文名:

抑郁相关

指标类型:

主要指标

Outcome:

Depression related indicator

Type:

Primary indicator

测量时间点:

测量方法:

后1周、1个月及6个月,由随访人员电话随访爱丁堡产后抑郁量表(中文版)和其他疼痛相关量表,随访人员需经过专业心理科医生的统一指导。

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:

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:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age 20 years
最大 Max age 40 years

性别:

女性

Gender:

Female

随机方法(请说明由何人用什么方法产生随机序列):

由专一人员采用随机信封法进行分组 薛杭医师:请说明何人使用何种方法(随机数字表?统计学软件?或其他)产生随机序列。

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

Grouped by a single person using the random envelope 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:

双盲

Blinding:

Double blind

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):

ResMan, http;//www.medresman.org.cn, 2021.12.31

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

ResMan, http;//www.medresman.org.cn, Dec.31st, 2021.

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:

使用病历记录表和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:

Use of medical records and electronic collection and management systems

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2020-03-10 10:14:36