ChiCTR-DCC-11001733 版本V1.2 版本创建时间2015/07/23 20:02:44 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:

ChiCTR-DCC-11001733 

最近更新日期:

Date of Last Refreshed on:

2015-07-23 20:01:21 

注册时间:

Date of Registration:

2011-11-28 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

核素导航联合染色法检测乳腺癌内乳前哨淋巴结的初步临床研究

Public title:

Lymphoscintigraphy Combine Staining in Diagnose of Internal Mammary Sentinel Lymph Nodes of Breast Cancer: A Pilot Clinical Study

注册题目简写:

English Acronym:

研究课题的正式科学名称:

核素导航联合染色法检测乳腺癌内乳前哨淋巴结的初步临床研究

Scientific title:

Lymphoscintigraphy Combine Staining in Diagnose of Internal Mammary Sentinel Lymph Nodes of Breast Cancer: A Pilot Clinical 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:

张在鸿 

研究负责人:

姜军 

Applicant:

ZaiHong Zhang 

Study leader:

Jun Jiang 

申请注册联系人电话:

Applicant telephone:

+86 023 68765633

研究负责人电话:

Study leader's
telephone:

+86 023 68765633

申请注册联系人传真 :

Applicant Fax:

+86 023 68765631

研究负责人传真:

Study leader's fax:

+86 023 68765631

申请注册联系人电子邮件:

Applicant E-mail:

64688700@qq.com

研究负责人电子邮件:

Study leader's E-mail:

jcbd@medmail.com.cn

申请单位网址(自愿提供):

Applicant website(voluntary supply):

http://web.swhospital.com/rxzx/

研究负责人网址(自愿提供):

Study leader's website(voluntary supply):

http://web.swhospital.com/rxzx/

申请注册联系人通讯地址:

第三军医大学西南医院乳腺疾病中心

研究负责人通讯地址:

第三军医大学西南医院乳腺疾病中心

Applicant address:

29 Gaotanyan Street, Shapingba District, Chongqing, China

Study leader's address:

29 Gaotanyan Street, Shapingba District, Chongqing, China

申请注册联系人邮政编码:

Applicant postcode:

400038

研究负责人邮政编码:

Study leader's postcode:

400038

申请人所在单位:

第三军医大学西南医院乳腺疾病中心

Applicant's institution:

Southwest Hospital, Third Military Medical 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:

KY201008

伦理委员会批件附件:

Approved file of Ethical Committee:

批准本研究的伦理委员会名称:

第三军医大学西南医院医学伦理委员会

Name of the ethic committee:

Ethics Committee of Southwest Hospital, Third Military Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2010-06-24 00:00:00

伦理委员会联系人:

Contact Name of the ethic committee:

伦理委员会联系地址:

Contact Address of the ethic committee:

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:

第三军医大学西南医院

Primary sponsor:

Southwest Hospital, Third Military Medical University

研究实施负责(组长)单位地址:

重庆市沙坪坝区高滩岩正街29号

Primary sponsor's address:

29 Gaotanyan Street, Shapingba District, Chongqing, 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):

重庆

市(区县):

Country:

China

Province:

Chongqing

City:

单位(医院):

第三军医大学西南医院

具体地址:

重庆市沙坪坝区高滩岩正街29号

Institution
hospital:

Southwest Hospital, Third Military Medical University

Address:

29 Gaotanyan Street, Shapingba District, Chongqing, China

经费或物资来源:

第三军医大学西南医院

Source(s) of funding:

Southwest Hospital, Third Military Medical University

研究疾病:

乳腺癌  

Target disease:

Breast cancer

研究疾病代码:

Target disease code:

研究类型:

诊断试验

Study type:

Diagnostic test

研究所处阶段:

I期临床试验 

Study phase:

1

研究设计:

诊断性病例对照试验 

Study design:

Diagnostic test: case-control 

研究目的:

1.分析两种联合法检测乳腺癌内乳前哨淋巴结的差异,探寻更有效的检测乳腺癌内乳前哨淋巴结的方法; 2.统计分析术后病理结果,探讨乳腺癌是否存在内乳前哨淋巴结及其活检术的临床应用价值。  

Objectives of Study:

1. The two methods of internal mammary sentinel lymph node detection of breast cancer were compared and analyzed in order to find a more effective method of detecting internal mammary lymph nodes of breast cancer; 2. Postoperative pathological results were statistically analyzed to explore whether internal mammary sentinel lymph nodes exist in breast cancer and the clinical value of internal mammary sentinel lymph node biopsy.

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.术前空心针穿刺活检证实为浸润性乳腺癌;
2.肿瘤为单侧、单发;
3.术前均行胸片、腹部超声及全身骨扫描检查确认无肺、肝及骨转移,必要时加行胸部或腹部CT或MRI;
4.肿瘤位于中央区、内侧区,或外侧区;
5.肿瘤大小≥5.0cm;
6.同侧腋窝淋巴结明显肿大互相融合或与其他组织粘连固定的;
7.临床B超、CT或核磁共振检查提示明显的内乳淋巴结肿大。
8.所有患者行均行术前新辅助化疗2-4疗程。
9.患者无其他部位恶性肿瘤病史。

Inclusion criteria

1. invasive breast cancer is confirmed by preoperative hollow needle aspiration biopsy;
2. the tumor is unilateral, single;
3. preoperative chest radiograph, abdominal ultrasound and systematic bone scan confirmed no metastases in lung, liver or bone, if necessary, additional chest or abdominal CT or MRI should be taken;
4. tumor is located in the central, medial or lateral area;
5. tumor size >=5.0 cm;
6. ipsilateral ALN are swollen, confluenced with each other or adhered with other tissue;
7. clinical ultrasound, CT or MRI shows remarkable IMN metastasis;
8. neoadjuvant chemotherapy for 2-4 courses before surgery;
9. no malignant tumor located in other sites of body.

排除标准:

1.有较严重的心肺疾病不能耐受手术者;
2.有胸膜与肺粘连或胸腔手术史;
3.炎性乳腺癌;
4.妊娠、哺乳期乳腺癌;
5.患者乳腺区域已接受过放射治疗。

Exclusion criteria:

1. with serious cardiac or pulmonary diseases, unable to tolerate the operation;
2. with pleura adhesion or lung adhesion or case history of thoracic operation;
3. inflammatory breast cancer;
4. breast cancer in pregnancy or lactation;
5. chemotherapy history in breast area.

研究实施时间:

Study execute time:

From 2010-06-24 00:00:00 To 2017-06-24 00:00:00  

征募观察对象时间:

Recruiting time:

From 2010-06-24 00:00:00 To 2012-06-24 00:00:00

诊断试验:

Diagnostic Tests:

金标准或参考标准(即可准确诊断某疾病的单项方法或多项联合方法,在本研究中用于诊断是否有该病的临床参考标准):

Gold Standard or Reference Standard (The clinical reference standards required to establish the presence or absence of the target condition in the tested population in present study):

指标试验(即本研究的待评估诊断试验,无论为方法、生物标志物或设备,均请列出名称):

Index test:

目标人群(可以是某种疾病患者或正常人群,详细描述其疾病特征,注意应纳入符合分布特点的全序列病例,具有良好的代表性)

例数:

Sample size:

Target condition (The target condition is a particular disease or disease stage that the index test will be intended to identify. Please specify the characteristics in detail; the population should has a complete spectrum and good representative):

容易混淆的疾病人群(即与目标疾病不易区分的一种或多种不同疾病,应避免采用正常人群对照的病例-对照设计):

例数:

Sample size:

Population with condition difficult to distinguish from the target condition, the normal population in a case-control study design should be avoid:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

重庆 

市(区县):

 

Country:

China

Province:

Chongqing

City:

单位(医院):

第三军医大学西南医院 

单位级别:

三级甲等 

Institution
hospital:

Southwest Hospital, Third Military Medical University

Level of the institution:

Tertiary A hospital

测量指标:

Outcomes:

指标中文名:

内乳前哨淋巴结检出率

指标类型:

主要指标

Outcome:

Internal mammary sentinel lymph node detection 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:

内乳淋巴结

组织:

内乳淋巴结

Sample Name:

Internal mammary lymph node

Tissue:

Internal mammary lymph node

人体标本去向

使用后销毁  

说明

30年

Fate of sample:

Destruction after use  

Note:

30years

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 70 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):

入院时间

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

Admission time

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

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):

第三军医大学西南医院

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

Southwest Hospital, Third Military Medical University

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:

第三军医大学西南医院

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

Southwest Hospital, Third Military Medical University

数据与安全监察委员会:

Data and Safety Monitoring Committee:

注册人:

Name of Registration:

 2015-07-23 20:01:21