ChiCTR2500109538 版本V1.0 版本创建时间2025/09/19 17:51:08 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:

ChiCTR2500109538 

最近更新日期:

Date of Last Refreshed on:

2025-09-19 17:50:35 

注册时间:

Date of Registration:

2025-09-19 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

吡仑帕奈口服混悬液治疗低龄儿童癫痫的多中心前瞻性观察性研究

Public title:

Perampanel Oral Suspension in the Treatment of Young Children with Epilepsy: A Multicenter Prospective Observational Study

注册题目简写:

吡仑帕奈口服混悬液用于低龄儿童癫痫

English Acronym:

perampanel oral suspension in young children with epilepsy

研究课题的正式科学名称:

吡仑帕奈口服混悬液治疗低龄儿童癫痫的多中心前瞻性观察性研究

Scientific title:

Perampanel Oral Suspension in the Treatment of Young Children with Epilepsy: A Multicenter Prospective Observational Study

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:

李栋梁 

研究负责人:

姜玉武 

Applicant:

Dongliang Li 

Study leader:

Yuwu Jiang 

申请注册联系人电话:

Applicant telephone:

+86 176 3984 3553

研究负责人电话:

Study leader's
telephone:

+86 176 3984 3553

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:

17639843553@163.com

研究负责人电子邮件:

Study leader's E-mail:

jiangyuwu@bjmu.edu.cn

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:

北京市大兴区乐园路5号,7号

研究负责人通讯地址:

北京市大兴区乐园路5号,7号

Applicant address:

No.5,7, Paradise Road, Daxing District, Beijing, China

Study leader's address:

No.5,7, Paradise Road, Daxing District, Beijing, 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:

北京大学第一医院

Applicant's institution:

Peking University First Hospital

研究负责人所在单位:

北京大学第一医院

Affiliation of the Leader:

Peking University First 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:

2025R0291-0003

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:

北京大学第一医院生物医学研究伦理委员会

Name of the ethic committee:

Peking University First Hospital Human Research Ethics Committee

伦理委员会批准日期:

Date of approved by ethic committee:

2025-09-03 00:00:00

伦理委员会联系人:

汪科

Contact Name of the ethic committee:

Ke Wang

伦理委员会联系地址:

北京市西城区西什库大街74号

Contact Address of the ethic committee:

No.74 Xishiku Street, Xicheng District, Beijing

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 10 6611 9025

伦理委员会联系人邮箱:

Contact email of the ethic committee:

bdyyll@126.com

研究实施负责(组长)单位:

北京大学第一医院

Primary sponsor:

Peking University First Hospital

研究实施负责(组长)单位地址:

北京市大兴区乐园路5号,7号

Primary sponsor's address:

No.5,7, Paradise Road, Daxing District, Beijing, 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):

北京

市(区县):

大兴区

Country:

China

Province:

Beijing

City:

Daxing district

单位(医院):

北京大学第一医院

具体地址:

北京市大兴区乐园路5号,7号

Institution
hospital:

Peking University First Hospital

Address:

No.5,7, Paradise Road, Daxing District, Beijing, China

经费或物资来源:

北京华夏公益基金会

Source(s) of funding:

Huahsia Foundation

研究疾病:

癫痫  

Target disease:

Epilepsy

研究疾病代码:

Target disease code:

研究类型:

观察性研究

Study type:

Observational study

研究所处阶段:

上市后药物 

Study phase:

4

研究设计:

队列研究 

Study design:

Cohort study 

研究目的:

观察吡仑帕奈口服混悬液添加治疗儿童癫痫的疗效和安全性  

Objectives of Study:

To observe the efficacy and safety of perampanel oral suspension as adjuntive treatment in children with epilepsy

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. 年龄在1 个月-4 岁,男性或女性; 2. 根据2017 年国际抗癫痫联盟(ILAE)癫痫发作和癫痫分类标准,被诊 断为癫痫; 3. 在就诊前3 个月至少有1 次癫痫发作; 4. 经医生判断适合吡仑帕奈口服混悬液添加治疗。

Inclusion criteria

1. Age between 1 month and 4 years old, male or female; 2. Diagnosed according to the 2017 International League Against Epilepsy (ILAE) classification criteria for Seizures and Epilepsy It was diagnosed as epilepsy. 3. At least one seizure in the 3 months before the visit; 4. Clinicians determined that perampanel oral suspension adjunctive treatment is suitable.

排除标准:

1. 已知对吡仑帕奈活性成分及口服混悬液辅料过敏; 2. 正在参加其他临床试验; 3. 研究者认为不能按时完成随访者。

Exclusion criteria:

1. Known to be allergic to the active ingredient of perampanel and the excipients of the oral suspension; 2. Participating in other clinical trials; 3. The investigator thought that the follow-up could not be completed on time.

研究实施时间:

Study execute time:

From 2025-09-21 00:00:00 To 2026-09-30 00:00:00  

征募观察对象时间:

Recruiting time:

From 2025-10-01 00:00:00 To 2026-04-30 00:00:00

干预措施:

Interventions:

组别:

吡仑帕奈组(吡仑帕奈口服混悬液添加治疗)

样本量:

122

Group:

Perampanel (perampanel oral suspension adjunctive treatment)

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

北京 

市(区县):

大兴区 

Country:

China

Province:

Beijing

City:

Daxing district

单位(医院):

北京大学第一医院 

单位级别:

三甲 

Institution
hospital:

Peking University First Hospital

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

北京 

市(区县):

 

Country:

China

Province:

Beijing

City:

单位(医院):

首都医科大学附属北京儿童医院 

单位级别:

三甲 

Institution
hospital:

Beijing Children's Hospital, Capital Medical University

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

上海 

市(区县):

 

Country:

China

Province:

Shanghai

City:

单位(医院):

复旦大学附属儿科医院 

单位级别:

三甲 

Institution
hospital:

Children's Hospital of Fudan University

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

深圳 

市(区县):

 

Country:

China

Province:

Shenzhen

City:

单位(医院):

深圳市儿童医院 

单位级别:

三甲 

Institution
hospital:

Shenzhen Children's Hospital

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

天津 

市(区县):

 

Country:

China

Province:

Tianjin

City:

单位(医院):

天津市儿童医院 

单位级别:

三甲 

Institution
hospital:

Tianjin Children's Hospital

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

陕西 

市(区县):

 

Country:

China

Province:

Shanxi

City:

单位(医院):

西安交通大学附属儿童医院 

单位级别:

三甲 

Institution
hospital:

Xi'an Children's Hospital

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

湖南 

市(区县):

 

Country:

China

Province:

Hunan

City:

单位(医院):

中南大学湘雅医院 

单位级别:

三甲 

Institution
hospital:

Xiangya Hospital of Central South University

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

重庆 

市(区县):

 

Country:

China

Province:

Chongqing

City:

单位(医院):

重庆医科大学附属儿童医院 

单位级别:

三甲 

Institution
hospital:

Children's Hospital of Chongqing Medical University

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

湖北 

市(区县):

 

Country:

China

Province:

Hubei

City:

单位(医院):

武汉儿童医院 

单位级别:

三甲 

Institution
hospital:

Wuhan Children's Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

50%有效率

指标类型:

主要指标

Outcome:

50% responder rate

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:

none

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 1M years
最大 Max age 4 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):

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

None

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:

Blinding:

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):

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:

EDC

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

EDC

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2025-09-19 17:50:35