ChiCTR2400092255 版本V1.0 版本创建时间2024/11/13 14:15:55 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:

ChiCTR2400092255 

最近更新日期:

Date of Last Refreshed on:

2024-11-13 14:15:26 

注册时间:

Date of Registration:

2024-11-13 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

IB2-IIA2期宫颈癌选择性腹主动脉旁淋巴清扫的模拟RCT研究

Public title:

Simulated RCT study of selective para-aortic lymphadenectomy for stage IB2-IIA2 cervical cancer

注册题目简写:

English Acronym:

研究课题的正式科学名称:

IB2-IIA2期宫颈癌选择性腹主动脉旁淋巴清扫的模拟RCT研究

Scientific title:

Simulated RCT study of selective para-aortic lymphadenectomy for stage IB2-IIA2 cervical cancer

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:

瞿欣瑜 

研究负责人:

邱君君 

Applicant:

Xinyu Qu 

Study leader:

Junjun Qiu 

申请注册联系人电话:

Applicant telephone:

+86 159 0187 5251

研究负责人电话:

Study leader's telephone:

+86 180 1773 8139

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:

quxinyu10027@fckyy.org.cn

研究负责人电子邮件:

Study leader's E-mail:

qiujunjun1113@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:

上海市杨浦区沈阳路128号

研究负责人通讯地址:

上海市杨浦区沈阳路128号

Applicant address:

No.128 Shenyang Road, Yangpu District, Shanghai

Study leader's address:

No.128 Shenyang Road, Yangpu District, Shanghai

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:

复旦大学附属妇产科医院

Applicant's institution:

Obstetrics & Gynecology Hospital of Fudan University

研究负责人所在单位:

复旦大学附属妇产科医院

Affiliation of the Leader:

Obstetrics & Gynecology Hospital of Fudan University

是否获伦理委员会批准:

是/Yes

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

妇产科伦审 2024-101

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:

复旦大学附属妇产科医院伦理委员会

Name of the ethic committee:

Ethics Committee of Obstetrics & Gynecology Hospital of Fudan University

伦理委员会批准日期:

Date of approved by ethic committee:

2024-06-03 00:00:00

伦理委员会联系人:

鞠丹丹

Contact Name of the ethic committee:

Dandan Ju

伦理委员会联系地址:

上海市黄浦区方斜路419号

Contact Address of the ethic committee:

No 419 Fangxie Road, Huangpu District, Shanghai

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 21 5351 3815

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:

复旦大学附属妇产科医院

Primary sponsor:

Obstetrics & Gynecology Hospital of Fudan University

研究实施负责(组长)单位地址:

上海市杨浦区沈阳路128号

Primary sponsor's address:

No 128 Shenyang 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):

Country:

China

Province:

Shanghai

City:

单位(医院):

复旦大学附属妇产科医院

具体地址:

上海市杨浦区沈阳路128号

Institution
hospital:

Obstetrics & Gynecology Hospital of Fudan University

Address:

No.128 Shenyang Road, Yangpu District, Shanghai

经费或物资来源:

上海申康医院发展中心

Source(s) of funding:

Shanghai Hospital Development Center

Target disease:

Cervical cancer

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:

队列研究 

Study design:

Cohort study 

研究目的:

1)研究PALN清扫术对宫颈癌IB2-IIA2期患者生存预后及生活质量的影响;(2)明确何时需行PALN清扫术,何时无需行PALN清扫术,为这一临床痛点提供真实世界证据,制定选择性PALN清扫策略,进一步完善宫颈癌精准分级手术治疗策略。  

Objectives of Study:

(1)To investigate the effects of PALN dissection on prognosis and quality of life of patients with stage IB2-IIA2 cervical cancer; (2) To clarify when PALN dissection is required, to provide real-world evidence for this clinical dilemma, to develop selective PALN dissection strategies, and to further improve the precise graded surgical treatment strategy for cervical cancer.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

纳入标准:临床诊断为宫颈癌(2018年FIGO分期:IB2-IIA2期);术前病理诊断为宫颈鳞癌、宫颈腺癌或宫颈腺鳞癌;年龄≤80岁;体力分级:Karnofsky评分≥60分;初次治疗者;受试者自愿加入本研究,签署知情同意书,依从性好,配合随访。

Inclusion criteria

Clinical diagnosis of cervical cancer (FIGO stage 2018: stage IB2-IIA2); Preoperative pathological diagnosis is cervical squamous cell carcinoma, cervical adenocarcinoma or cervical adenocarcinoma; Age <=80 years old; Physical strength rating: Karnofsky score >=60 points; Primarily treated; Participants who voluntarily join the study, sign informed consent with good compliance.

排除标准:

一般情况差,严重内科合并症难以耐受手术治疗者;既往接受盆腔/腹部放疗照射或化疗的患者;妊娠期患者;合并其他妇科恶性疾病如卵巢肿瘤的患者;CT、MRI或PET提示子宫颈外转移;不能或不愿意签署知情同意书者,不能或不愿意遵守研究要求者。

Exclusion criteria:

Patients with poor general condition and severe medical complications that are difficult to tolerate surgical treatment; Patients who have previously received pelvic/abdominal radiation or chemotherapy; Pregnant patients; Patients with other gynecological malignancies such as ovarian tumors; CT, MRI or PET suggest extrinsic cervical metastasis; Unable or unwilling to sign informed consent, unable or unwilling to comply with research requirements.

研究实施时间:

Study execute time:

From 2024-06-05 00:00:00 To 2025-09-30 00:00:00  

征募观察对象时间:

Recruiting time:

From 2024-06-05 00:00:00 To 2025-09-30 00:00:00  

干预措施:

Interventions:

组别:

试验组(根治性手术+腹主动脉旁淋巴结清扫)

样本量:

355

Group:

Experimental group (Radical surgery + para-aortic lymph node dissection)

Sample size:

干预措施:

干预措施代码:

Intervention:

none

Intervention code:

组别:

对照组(根治性手术)

样本量:

355

Group:

Control group (Radical surgery)

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):

上海 

市(区县):

 

Country:

China 

Province:

Shanghai 

City:

 

单位(医院):

复旦大学附属妇产科医院 

单位级别:

三甲 

Institution
hospital:

Obstetrics & Gynecology Hospital of Fudan University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

总体生存率

指标类型:

主要指标

Outcome:

overall survival

Type:

Primary indicator

测量时间点:

2年、5年

测量方法:

Measure time point of outcome:

2-year, 5-year

Measure method:

指标中文名:

无进展生存率

指标类型:

主要指标

Outcome:

Progression-free survival

Type:

Primary indicator

测量时间点:

2年、5年

测量方法:

Measure time point of outcome:

2-year, 5-year

Measure method:

指标中文名:

生活质量

指标类型:

次要指标

Outcome:

quality of life

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:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 80 years

性别:

女性

Gender:

Female

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

Yes

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6个月内,联系研究者索取

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

Within 6 months following the completion of the study, please contact the researcher to request the information.

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:

CRF

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

CRF

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:

 2024-11-13 14:15:26