ChiCTR2500100659 版本V1.0 版本创建时间2025/04/14 08:41:19 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:

ChiCTR2500100659 

最近更新日期:

Date of Last Refreshed on:

2025-04-14 08:40:32 

注册时间:

Date of Registration:

2025-04-14 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

经静脉入路(TVE)治疗脑动静脉畸形的前瞻性多中心临床注册登记研究

Public title:

A prospective multicenter clinical registry study of transvenous approach (TVE) for the treatment of cerebral arteriovenous malformations

注册题目简写:

English Acronym:

研究课题的正式科学名称:

经静脉入路(TVE)治疗bAVM的前瞻性多中心临床注册登记研究

Scientific title:

A prospective multicenter clinical registry study of transvenous approach (TVE) for the treatment of cerebral arteriovenous malformations

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:

尚成浩 

研究负责人:

刘建民 

Applicant:

Chenghao Shang 

Study leader:

Jianmin Liu 

申请注册联系人电话:

Applicant telephone:

+86 186 0176 2436

研究负责人电话:

Study leader's
telephone:

+86 139 0178 0638

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:

sch951219@163.com

研究负责人电子邮件:

Study leader's E-mail:

liu118@vip.163.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:

上海市杨浦区长海路168号

研究负责人通讯地址:

上海市杨浦区长海路168号

Applicant address:

No. 168, Changhai Road, Yangpu District, Shanghai

Study leader's address:

No. 168, Changhai Road, Yangpu District, Shanghai

申请注册联系人邮政编码:

Applicant postcode:

200433

研究负责人邮政编码:

Study leader's postcode:

200433

申请人所在单位:

海军军医大学第一附属医院(上海长海医院)

Applicant's institution:

The First Affiliated Hospital of Naval Medical University (Shanghai Changhai Hospital)

研究负责人所在单位:

海军军医大学第一附属医院(上海长海医院)

Affiliation of the Leader:

The First Affiliated Hospital of Naval Medical University (Shanghai Changhai 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:

CHEC2025-097

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:

上海长海医院医学伦理委员会

Name of the ethic committee:

Shanghai Changhai Hospital Medical Ethics Committee

伦理委员会批准日期:

Date of approved by ethic committee:

2025-03-14 00:00:00

伦理委员会联系人:

张优琴

Contact Name of the ethic committee:

Youqin Zhang

伦理委员会联系地址:

上海市杨浦区长海路168号

Contact Address of the ethic committee:

No. 168, Changhai Road, Yangpu District, Shanghai

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 139 1835 5518

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:

海军军医大学第一附属医院(上海长海医院)

Primary sponsor:

The First Affiliated Hospital of Naval Medical University (Shanghai Changhai Hospital)

研究实施负责(组长)单位地址:

上海市杨浦区长海路168号

Primary sponsor's address:

No. 168, Changhai Road, Yangpu District, Shanghai

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

上海市

市(区县):

上海市

Country:

China

Province:

Shanghai

City:

Shanghai

单位(医院):

海军军医大学第一附属医院(上海长海医院)

具体地址:

上海市杨浦区长海路168号

Institution
hospital:

The First Affiliated Hospital of Naval Medical University (Shanghai Changhai Hospital)

Address:

No. 168, Changhai Road, Yangpu District, Shanghai

经费或物资来源:

上海市申康医学中心

Source(s) of funding:

Shanghai Shenkang Medical Center

研究疾病:

脑动静脉畸形  

Target disease:

Cerebral arteriovenous malformations

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.研究确定TVE治疗BAVM的安全性和有效性, 2.确立经静脉入路栓塞治疗的脑动静脉畸形的病例选择标准; 3.研究形成TVE治疗BAVM的标准技术规范流程,并进行推广应用;  

Objectives of Study:

1. To determine the safety and efficacy of TVE in the treatment of BAVM, 2. Establish the case selection criteria for cerebral arteriovenous malformations treated by intravenous embolization; 3. Research and form a standard technical specification process for the treatment of BAVM with TVE, and promote its application;

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、 BAVM诊断明确:具有症状、经MR/CTA/DSA明确BAVM诊断 。 2、年龄>=13岁<=60岁; 3、 单支或两支优势静脉引流; 4、TVE时畸形团直径<3.5cm; 5、取得研究参与者本人或其法定监护人或代表签署知情同意书。

Inclusion criteria

1.Diagnosis of BAVM: Diagnosis of BAVM is confirmed by MR/CTA/DSA. 2.Age≥ 13 years old ≤ 60 years old; 3. single or two dominant venous drainage; 4.The diameter of the deformity during TVE< 3.5cm; 5.Obtain informed consent signed by the research participant or his/her legal guardian or representative.

排除标准:

1、怀孕或哺乳期;尿或血浆孕检阳性的绝经期前女性患者(无有记录的外科绝育史); 2、入院时双侧瞳孔散大的患者; 3、合并肿瘤、出血性疾病或其他已知的严重基础疾病(如慢阻肺、多脏器功能不全、严重 糖尿病、心功能不全和慢性肾疾病等); 4、治疗前颅内出血或神经功能障碍致mRS≥3分 5、放射影像证实的合并破裂动脉瘤病; 6、bAVM过于弥散; 7、血小板计数<1000,000; 8、INR > 1.4,或TP或ATPP升高;需长期抗凝的患者; 9、其他不适合入组情况(由两名医生评定后决定); 10、参加其他临床研究患者 。

Exclusion criteria:

1.Pregnancy or lactation; Premenopausal female patients with positive urine or plasma pregnancy test (no documented history of surgical sterilization); 2.Patients with bilateral mydriasis at the time of admission; 3.Combined tumors, bleeding disorders or other known serious underlying diseases (such as chronic obstructive pulmonary disease, multi-organ insufficiency, severe diabetes, cardiac insufficiency and chronic kidney disease, etc.); 4.mRS ≥ 3 points due to intracranial hemorrhage or neurological dysfunction before treatment 5.Radiological image confirmed with ruptured aneurysm; 6.The bAVM is too diffuse; 7.Platelet count< 1000,000; 8.INR > 1.4, or elevated TP or ATPP; Patients requiring long-term anticoagulation; 9.Other conditions that are not suitable for enrollment (determined by two doctors); 10. Patients participating in other clinical studies.

研究实施时间:

Study execute time:

From 2023-09-01 00:00:00 To 2026-08-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2025-04-18 00:00:00 To 2026-08-31 00:00:00

干预措施:

Interventions:

组别:

经静脉入路介入栓塞治疗组

样本量:

86

Group:

Transvenous interventional embolization treatment group

Sample size:

干预措施:

经静脉入路栓塞治疗

干预措施代码:

Intervention:

Transvenous embolization therapy

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

上海市 

市(区县):

上海市 

Country:

China

Province:

Shanghai

City:

Shanghai

单位(医院):

海军军医大学第一附属医院(上海长海医院) 

单位级别:

三甲 

Institution
hospital:

The First Affiliated Hospital of Naval Medical University (Shanghai Changhai Hospital)

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

上海市 

市(区县):

上海市 

Country:

China

Province:

Shanghai

City:

单位(医院):

复旦大学附属华山医院 

单位级别:

三甲 

Institution
hospital:

Huashan Hospital Affiliated to Fudan University

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

上海市 

市(区县):

上海市 

Country:

China

Province:

Shanghai

City:

单位(医院):

上海市第一人民医院 

单位级别:

三甲 

Institution
hospital:

Shanghai First People's Hospital

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

上海市 

市(区县):

上海市 

Country:

China

Province:

Shanghai

City:

单位(医院):

上海交通大学医学院附 属第九人民医院 

单位级别:

三甲 

Institution
hospital:

The Ninth People's Hospital affiliated to Shanghai Jiao Tong University School of Medicine

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

上海市 

市(区县):

上海市 

Country:

China

Province:

Shanghai

City:

单位(医院):

上海市第四人民医院 

单位级别:

二级 

Institution
hospital:

Shanghai Fourth People's Hospital

Level of the institution:

Secondary

测量指标:

Outcomes:

指标中文名:

入组180天(6个月)后神经功能预后良好率

指标类型:

主要指标

Outcome:

Good prognosis rate of neurological function after 180 days (6 months) of enrollment

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

术后即刻完全闭塞率

指标类型:

次要指标

Outcome:

Immediate complete occlusion rate postoperatively

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

术后6月脑血管造影BAVM闭塞率

指标类型:

次要指标

Outcome:

BAVM occlusion rate of cerebral angiography at 6 months after surgery

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

入组至栓塞结束后一周以内的卒中事件

指标类型:

次要指标

Outcome:

Stroke events within one week of enrollment to the end of embolization

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

栓塞一周后至1年临床随访中的卒中事件

指标类型:

次要指标

Outcome:

Stroke events at clinical follow-up one week after embolization to 1 year

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:

组织:

Sample Name:

None

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 13 years
最大 Max age 60 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:

不公开/Private

盲法:

Blinding:

None

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):

研究结束后2年(2028.08)将数据公布在邮箱duanguoli2008@163.com

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

The data will be published in the mailbox 2 years after the end duanguoli2008@163.com of the study (2028.08).

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:

暂未确定/Not yet

注册人:

Name of Registration:

 2025-04-14 08:40:32