ChiCTR2500106997 版本V1.0 版本创建时间2025/08/01 12:20:09 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:

ChiCTR2500106997 

最近更新日期:

Date of Last Refreshed on:

2025-08-01 12:20:01 

注册时间:

Date of Registration:

2025-08-01 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

盐酸伊立替康脂质体注射液(II)治疗胆道系统恶性肿瘤真实世界非干预性临床病例收集

Public title:

Irinotecan Hydrochloride Liposome Injection (II) in the Treatment of Malignant Tumors of the Biliary Tract: A Collection of Real-World Non-Interventional Clinical Cases

注册题目简写:

English Acronym:

研究课题的正式科学名称:

盐酸伊立替康脂质体注射液(II)治疗胆道系统恶性肿瘤真实世界非干预性临床病例收集

Scientific title:

Irinotecan Hydrochloride Liposome Injection (II) in the Treatment of Malignant Tumors of the Biliary Tract: A Collection of Real-World Non-Interventional Clinical Cases

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:

程颖 

研究负责人:

钱军/程颖 

Applicant:

Cheng Ying 

Study leader:

Qian Jun / Cheng Ying 

申请注册联系人电话:

Applicant telephone:

+86 153 6504 6886

研究负责人电话:

Study leader's
telephone:

+86 153 6504 6886

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:

chengyin82@163.com

研究负责人电子邮件:

Study leader's E-mail:

chengyin82@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:

江苏省南京市秦淮区汉中路155号

研究负责人通讯地址:

江苏省南京市秦淮区汉中路155号

Applicant address:

No. 155 Hanzhong Road, Qinhuai District, Nanjing City, Jiangsu Province, China

Study leader's address:

No. 155 Hanzhong Road, Qinhuai District, Nanjing City, Jiangsu Province, 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:

江苏省中医院

Applicant's institution:

Jiangsu Province Hospital of Chinese Medicine

研究负责人所在单位:

江苏省中医院

Affiliation of the Leader:

Jiangsu Province Hospital of Chinese Medicine

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:

2025NL-089-02

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:

南京中医药大学附属医院(江苏省中医院)伦理委员会

Name of the ethic committee:

Ethics Committee of the Affiliated Hospital of Nanjing University of Chinese Medicine (Jiangsu Provincial Hospital of Traditional Chinese Medicine)

伦理委员会批准日期:

Date of approved by ethic committee:

2025-04-25 00:00:00

伦理委员会联系人:

王卯

Contact Name of the ethic committee:

Wang Mao

伦理委员会联系地址:

江苏省南京市秦淮区汉中路155号

Contact Address of the ethic committee:

No. 155 Hanzhong Road, Qinhuai District, Nanjing City, Jiangsu Province, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 25 8656 0515

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:

江苏省中医院

Primary sponsor:

Jiangsu Province Hospital of Chinese Medicine

研究实施负责(组长)单位地址:

江苏省南京市秦淮区汉中路155号

Primary sponsor's address:

No. 155 Hanzhong Road, Qinhuai District, Nanjing City, Jiangsu Province, 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):

江苏

市(区县):

Country:

China

Province:

Jiangsu

City:

单位(医院):

江苏省中医院

具体地址:

江苏省南京市秦淮区汉中路155号

Institution
hospital:

Jiangsu Province Hospital of Chinese Medicine

Address:

No. 155 Hanzhong Road, Qinhuai District, Nanjing City, Jiangsu Province, China

经费或物资来源:

自筹

Source(s) of funding:

Self-financed

研究疾病:

胆道系统恶性肿瘤  

Target disease:

Biliary Tract Cancer

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:

其它 

Study phase:

N/A

研究设计:

病例研究 

Study design:

Case study 

研究目的:

评价盐酸伊立替康脂质体注射液(II)治疗胆道系统恶性肿瘤的疗效与安全性  

Objectives of Study:

Evaluate the efficacy and safety of Irinotecan Hydrochloride Liposome Injection (II) in the treatment of malignant tumors of the biliary tract system

药物成份或治疗方案详述:

使用盐酸伊立替康脂质体注射液(II)二线/三线治疗胆道系统恶性肿瘤 

Description for medicine or protocol of treatment in detail:

Using irinotecan hydrochloride liposome injection (II) as second-line/third-line treatment for malignant tumors of the biliary tract system 

纳入标准:

1. 病理诊断确诊的不可切除或转移性BTC患者 2. 年龄18~75周岁,男女不限 3. ECOG评分0~2分 4. 预期生存时间≥12周 5. 至少有一个可测量病灶(RECIST1.1 标准) 6. BTC二线/三线治疗过程中使用过伊立替康脂质体(II) 7. 有完整的伊立替康脂质体(II)使用记录 8. 充分了解本研究,自愿参与并签署知情同意书

Inclusion criteria

1. Patients with pathologically confirmed unresectable or metastatic BTC 2. Aged 18–75 years, regardless of gender 3. ECOG score of 0–2 4. Expected survival time >= 12 weeks 5. At least one measurable lesion (RECIST 1.1 criteria) 6. Received liposomal irinotecan (II) during second-/third-line treatment for BTC 7. Complete records of liposomal irinotecan (II) administration available 8. Fully informed about the study, voluntarily participate, and sign the informed consent form

排除标准:

1. 既往5年内诊断有其他恶性肿瘤 2. 存在不可控的远处转移,如脑转移 3. 接受过肝移植 4. 发生肝脏转移且转移灶占肝脏总体积的50%及以上 5. 病例资料不完整,影响疗效与安全性评估

Exclusion criteria:

1. Diagnosed with other malignant tumors within the past 5 years 2. Presence of uncontrolled distant metastases, such as brain metastases 3. History of liver transplantation 4. Liver metastases occupying 50% or more of the total liver volume 5. Incomplete case data affecting efficacy and safety evaluation

研究实施时间:

Study execute time:

From 2025-01-01 00:00:00 To 2026-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2025-08-01 00:00:00 To 2026-12-31 00:00:00

干预措施:

Interventions:

组别:

观察组

样本量:

30

Group:

Observation group

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):

江苏 

市(区县):

 

Country:

China

Province:

Jiangsu

City:

单位(医院):

江苏省中医院 

单位级别:

三甲 

Institution
hospital:

Jiangsu Province Hospital of Chinese Medicine

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

无进展生存期

指标类型:

主要指标

Outcome:

Progression-free survival

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

疾病控制率

指标类型:

次要指标

Outcome:

Disease control rate

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

1年生存率

指标类型:

次要指标

Outcome:

1-year S.R.

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:

Sample Name:

Blood

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 18 years
最大 Max age 75 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):

不共享

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

Do not share

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:

病例记录表记录

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

Case Report Form Recording

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:

 2025-08-01 12:20:01