ChiCTR2200062242 版本V1.0 版本创建时间2022/07/31 00:18:55 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:

ChiCTR2200062242 

最近更新日期:

Date of Last Refreshed on:

2022-07-31 00:18:27 

注册时间:

Date of Registration:

2022-07-31 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

基于稀疏血药浓度的癫痫患者丙戊酸盐群体药动学模型构建

Public title:

The development of individualized medication model of valproic acid in epileptic based on sparse plasma drug concentration

注册题目简写:

English Acronym:

研究课题的正式科学名称:

基于稀疏血药浓度的癫痫患者丙戊酸盐群体药动学模型构建

Scientific title:

The development of individualized medication model of valproic acid in epileptic based on sparse plasma drug concentration

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:

孙媛媛 

研究负责人:

阳国平 

Applicant:

Yuanyuan Sun 

Study leader:

Guoping Yang 

申请注册联系人电话:

Applicant telephone:

13236916265

研究负责人电话:

Study leader's
telephone:

13974817168

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:

syy09826@163.om

研究负责人电子邮件:

Study leader's E-mail:

syy09826@163.om

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:

湖南省长沙市岳麓区桐梓坡路138号

研究负责人通讯地址:

湖南省长沙市岳麓区桐梓坡路138号中南大学湘雅三医院

Applicant address:

138 Tongzipo Road, Yuelu District, Changsha, Hu'nan, China

Study leader's address:

The Third Xiangya Hospital, Central South University, 138 Tongzipo Road, Yuelu District, Changsha, Hunan, 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:

中南大学湘雅三医院临床试验研究中心

Applicant's institution:

Center for Clinical Pharmacology, The Third Xiangya Hospital, Central South University

研究负责人所在单位:

Affiliation of the Leader:

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:

快I 22049

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:

中南大学湘雅三医院伦理委员会

Name of the ethic committee:

IRB, The Third Xiangya Hospital, Central South University

伦理委员会批准日期:

Date of approved by ethic committee:

2013-03-22 00:00:00

伦理委员会联系人:

王晓敏

Contact Name of the ethic committee:

Xiaomin Wang

伦理委员会联系地址:

湖南省长沙市岳麓区桐梓坡路138号中南大学湘雅三医院伦理委员会

Contact Address of the ethic committee:

RB, The Third Xiangya Hospital, Central South University, 138 Tongzipo Road, Yuelu District, Changsha, Hunan, 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:

中南大学湘雅三医院临床试验研究中心

Primary sponsor:

Center for Clinical Pharmacology, The Third Xiangya Hospital, Central South University

研究实施负责(组长)单位地址:

湖南省长沙市岳麓区桐梓坡路138号

Primary sponsor's address:

138 Tongzipo Road, Yuelu District, Changsha, Hu'nan, 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):

湖南

市(区县):

长沙

Country:

China

Province:

Hu'nan

City:

Changsha

单位(医院):

中南大学湘雅三医院

具体地址:

岳麓区桐梓坡路138号

Institution
hospital:

The Third Xiangya Hospital, Central South University

Address:

138 Tongzipo Road, Yuelu District

经费或物资来源:

课题基金

Source(s) of funding:

Sustentation Funds

研究疾病:

癫痫  

Target disease:

Epileptic

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:

横断面 

Study design:

Cross-sectional 

研究目的:

本研究旨在建立癫痫患者中基于稀疏血药浓度的丙戊酸钠、丙戊酸镁(下文合称丙戊酸盐)个体化用药模型  

Objectives of Study:

This study aimed to develop an individualized medication model of valproic acid in epileptic based on sparse plasma drug concentration

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)使用丙戊酸盐片剂、丙戊酸盐缓释片或丙戊酸盐注射液的癫痫患者;
(2)达到稳态浓度(口服丙戊酸盐连续用药时间>7天或注射液连续用药时间>3天);
(3)签署知情同意书。

Inclusion criteria

(1) epileptic patients using valproate tablets, valproate sustained-release tablets or valproate injection;

(2) steady state concentration (oral valproate continuous administration time >7 days or injection continuous administration time >3 days);

(3) Signed informed consent.

排除标准:

(1)肝肾功能异常的患者;
(2)除抗癫痫药物外,合并使用其他会影响丙戊酸盐血药浓度的药物的患者。

Exclusion criteria:

(1) Patients with abnormal liver and kidney function;

(2) In addition to antiepileptic drugs, patients with concomitant use of other drugs that may affect the plasma concentration of valproate.

研究实施时间:

Study execute time:

From 2022-07-30 00:00:00 To 2022-10-30 00:00:00  

征募观察对象时间:

Recruiting time:

From 2022-07-30 00:00:00 To 2022-10-30 00:00:00

干预措施:

Interventions:

组别:

试验组

样本量:

50

Group:

Experimental group

Sample size:

干预措施:

丙戊酸盐片剂、丙戊酸盐缓释片或丙戊酸盐注射液

干预措施代码:

Intervention:

Valproate tablets, valproate sustained-release tablets or valproate injection

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

湖南 

市(区县):

长沙 

Country:

China

Province:

Hu'nan

City:

Changsha

单位(医院):

中南大学湘雅三医院 

单位级别:

三级甲等 

Institution
hospital:

The Third Xiangya Hospital, Central South University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

丙戊酸血浆药物浓度

指标类型:

主要指标

Outcome:

Valproic acid concentration in plasma

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:

血浆

组织:

Sample Name:

Plasma

Tissue:

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:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age 0 years
最大 Max age 100 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):

按照入组顺序

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

In the order of entry

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:

NA

Blinding:

NA

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):

NA

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

NA

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:

有/Yes

注册人:

Name of Registration:

 2022-07-31 00:18:28