艾司氯胺酮MECT治疗难治性双相抑郁

注册号:

Registration number:

ChiCTR2000040082 

最近更新日期:

Date of Last Refreshed on:

2024-05-06 17:56:46 

注册时间:

Date of Registration:

2020-11-20 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

艾司氯胺酮MECT治疗难治性双相抑郁

Public title:

Adjunctive esketamine and MECT for treatment-refractory bipolar depression

注册题目简写:

English Acronym:

研究课题的正式科学名称:

改良电抽搐治疗难治性抑郁症的研究

Scientific title:

An exploratory study of adjunctive modified electroconvulsive therapy for treatment-resistant 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:

郑伟 

研究负责人:

黄雄 

Applicant:

Wei Zheng 

Study leader:

Xiong Huang 

申请注册联系人电话:

Applicant telephone:

+86 020-81268169

研究负责人电话:

Study leader's
telephone:

+86 020-81268169

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:

zhengwei0702@163.com

研究负责人电子邮件:

Study leader's E-mail:

1195768576@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:

广东省广州市荔湾区明心路36号

研究负责人通讯地址:

广东省广州市荔湾区明心路36号

Applicant address:

36 Mingxin Road, Liwan District, Guangzhou, Guangdong, China

Study leader's address:

36 Mingxin Road, Liwan District, Guangzhou, Guangdong, 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:

广州医科大学附属脑科医院(广州市惠爱医院)

Applicant's institution:

The Affiliated Brain Hospital of Guangzhou Medical University (Guangzhou Huiai Hospital)

研究负责人所在单位:

广州医科大学附属脑科医院(广州市惠爱医院)

Affiliation of the Leader:

The Affiliated Brain Hospital of Guangzhou Medical University (Guangzhou Huiai Hospital)

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:

(2020)第(023)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:

广州医科大学附属脑科医院伦理委员会

Name of the ethic committee:

The Ethics Committee of the Affiliated Brain Hospital of Guangzhou Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2020-05-25 00:00:00

伦理委员会联系人:

杨婵娟

Contact Name of the ethic committee:

Chan-Juan Yang

伦理委员会联系地址:

广东省广州市荔湾区明心路36号

Contact Address of the ethic committee:

36 Mingxin Road, Liwan District, Guangzhou, Guangdong, 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:

广州医科大学附属脑科医院(广州市惠爱医院)

Primary sponsor:

The Affiliated Brain Hospital of Guangzhou Medical University (Guangzhou Huiai Hospital)

研究实施负责(组长)单位地址:

广东省广州市荔湾区明心路36号

Primary sponsor's address:

36 Mingxin Road, Liwan District, Guangzhou, Guangdong, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

省(直辖市):

市(区县):

Country:

Province:

City:

单位(医院):

具体地址:

Institution
hospital:

Address:

经费或物资来源:

广州市临床特色技术项目

Source(s) of funding:

Guangzhou Clinical characteristic Technology Project

研究疾病:

双相情感障碍  

Target disease:

treatment-refractory bipolar disorder

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:

单臂 

Study design:

Single arm 

研究目的:

(1)探讨艾司氯胺酮作为MECT麻醉剂治疗难治性双相抑郁(TRBD)的疗效和安全性研究;(2)探讨艾司氯胺酮作为MECT麻醉剂治疗TRBD的临床疗效相关预测指标。  

Objectives of Study:

(1) To explore the efficacy and safety of esmketamine as modified electroconvulsive therapy anesthetic in the treatment of treatment-refractory bipolar depression (TRBD); (2) To examine the clinical efficacy predictive factor of esmketamine as MECT anesthetic for TRBD.

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患有符合DSM-IV诊断标准的其他重性精神障碍,包括器质性精神障碍、酒精依赖,毒品依赖/滥用、精神分裂症等;
②严重躯体或脑器质性疾病史,颅脑外伤史及癫痫病史,韦氏智力测验(WAIS-RC)的全量表智商(FIQ≤80);
③药物、酒精或其他精神活性物质滥用史;
④体内带有金属者,如起搏器或脑内电极;
⑤既往麻醉剂过敏史;
⑥怀孕或哺乳期;
⑦有磁共振检查禁忌症者或不能耐受MRI扫描环境者如幽闭恐惧症;
⑧近三个月接受MECT治疗,主管医生从治疗角度认为不适合进行MECT治疗。

Exclusion criteria:

(1) Other major psychiatric disorders that meet the DSM-IV diagnostic criteria include organic mental disorders, alcohol dependence, drug dependence/abuse, schizophrenia, etc;
(2) Currently, there are serious and unstable somatic diseases such as diabetes, thyroid disease, hypertension, heart disease and narrow-angle glaucoma, etc; Wechsler intelligence test (WAIS-RC) full scale IQ (FIQ) total scores <= 80;
(3) A history of neurological diseases such as epilepsy and dementia;
(4) Subjects with metal in the body, such as pacemaker or brain electrode;
(5) Previous history of anesthetics allergy;
(6) Women who are at the stage of pre-pregnancy, pregnancy or lataction;
(7) Contraindications to MRI or intolerant of MRI scanning environment, such as claustrophobia;
(8) MECT treatment in the past three months, the doctor in charge thinks that MECT is not suitable for treatment.

研究实施时间:

Study execute time:

From 2020-10-16 00:00:00 To 2024-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2020-11-20 00:00:00 To 2024-12-31 00:00:00

干预措施:

Interventions:

组别:

Case series

样本量:

50

Group:

Case series

Sample size:

干预措施:

艾司氯胺酮

干预措施代码:

Intervention:

esmketamine

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

广东省 

市(区县):

 

Country:

China

Province:

Guangdong

City:

单位(医院):

广州医科大学附属脑科医院(广州市惠爱医院) 

单位级别:

三甲医院 

Institution
hospital:

The Affiliated Brain Hospital of Guangzhou Medical University (Guangzhou Huiai Hospital)

Level of the institution:

Tertiary A Hospital

测量指标:

Outcomes:

指标中文名:

疗效

指标类型:

主要指标

Outcome:

Efficacy

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

安全性

指标类型:

次要指标

Outcome:

safety

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

认知功能

指标类型:

次要指标

Outcome:

Cognitive function

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:

血液

组织:

静脉

Sample Name:

Blood

Tissue:

Vein

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

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 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):

由临床研究人员连续入组符合入组标准的患者

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

No

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:

N/A

Blinding:

N/A

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):

Not stated

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

Not stated

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:

Not stated

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:

 2020-11-20 22:26:38