ChiCTR2400093940 版本V1.0 版本创建时间2024/12/13 15:26:39 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:

ChiCTR2400093940 

最近更新日期:

Date of Last Refreshed on:

2024-12-13 15:26:12 

注册时间:

Date of Registration:

2024-12-13 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

中医药延缓非小细胞肺癌EGFR-TKIs耐药的方案应用与推广

Public title:

Application and promotion of traditional Chinese medicine to delay the resistance of EGFR-TKIs in non-small cell lung cancer

注册题目简写:

English Acronym:

研究课题的正式科学名称:

中医药延缓非小细胞肺癌EGFR-TKIs耐药的方案应用与推广

Scientific title:

Application and promotion of traditional Chinese medicine to delay the resistance of EGFR-TKIs in non-small cell lung cancer

研究课题代号(代码):

Study subject ID:

21MC1930500

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:

王中奇 

研究负责人:

王中奇 

Applicant:

Wang Zhongqi 

Study leader:

Wang Zhongqi 

申请注册联系人电话:

Applicant telephone:

+86 136 3662 3819

研究负责人电话:

Study leader's telephone:

+86 136 3662 3819

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:

aledx@sina.com

研究负责人电子邮件:

Study leader's E-mail:

aledx@sina.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:

上海市徐汇区宛平南路725号

研究负责人通讯地址:

上海市徐汇区宛平南路725号

Applicant address:

725 Wanping Road South, Xuhui District, Shanghai, China

Study leader's address:

725 Wanping Road South, Xuhui District, Shanghai, 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:

上海中医药大学附属龙华医院

Applicant's institution:

Longhua Hospital, Shanghai University of Traditional Chinese Medicine

研究负责人所在单位:

上海中医药大学附属龙华医院

Affiliation of the Leader:

Longhua Hospital, Shanghai University of Traditional Chinese Medicine

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:

2022LCSY013号

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:

上海中医药大学附属龙华医院医学伦理委员会

Name of the ethic committee:

Ethics Committee of Longhua Hospital, Shanghai University of Traditional Chinese Medicine

伦理委员会批准日期:

Date of approved by ethic committee:

2022-04-28 00:00:00

伦理委员会联系人:

陈小芸

Contact Name of the ethic committee:

Chen Xiaoyun

伦理委员会联系地址:

上海徐汇区宛平南路725号

Contact Address of the ethic committee:

725 Wanping Road South, Xuhui District, Shanghai, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 64385700

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:

上海中医药大学附属龙华医院

Primary sponsor:

Longhua Hospital, Shanghai University of Traditional Chinese Medicine

研究实施负责(组长)单位地址:

上海市徐汇区宛平南路725号

Primary sponsor's address:

725 Wanping Road South, Xuhui District, Shanghai, 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):

上海

市(区县):

徐汇区

Country:

China

Province:

Shanghai

City:

Xuhui District

单位(医院):

上海中医药大学附属龙华医院

具体地址:

徐汇区宛平南路725号

Institution
hospital:

Longhua Hospital, Shanghai University of Traditional Chinese Medicine

Address:

725 Wanping Road South, Xuhui District

经费或物资来源:

上海市科学技术委员会

Source(s) of funding:

Shanghai Municipal Science and Technology Commission

Target disease:

lung cancer

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

探索性研究/预试验 

Study phase:

0

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

完成肺岩宁方延缓EGFR-TKI耐药临床疗效的客观评价,制定益气养精散结法抑制EGFR-TKI耐药的治疗方案,为肺岩宁的中药新药研发奠定可靠的基础。  

Objectives of Study:

To complete objective evaluation of the clinical efficacy of Feiyanning prescription for delaying EGFR-TKI resistance, and the therapeutic schedule for inhibiting EGFR-TKI resistance by Yiqi Yangjing Sanjie method, laying a reliable foundation for the development of Feiyanning as a new Chinese medicine.

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)病理或细胞学确诊为III-IV期肺腺癌患者或术后复发转移者; (2)EGFR检测敏感型(18、19、21号外显子有突变,20外显子无突变); (3)符合中医证型标准者; (4)年龄>18岁,且≤75岁的患者; (5)体能状况评分≤2分; (6)血象心肝肾功能正常范围; (7)签署知情同意书。

Inclusion criteria

(1) Patients diagnosed with stage III-IV lung adenocarcinoma by pathology or cytology, or those with postoperative recurrence and metastasis; (2) EGFR detection sensitive type (with mutations in exons 18, 19, and 21, and no mutation in exon 20); (3) Those who meet the criteria of traditional Chinese medicine syndrome types; (4) Patients aged over 18 years and <= 75 years old; (5) Physical fitness score <= 2 points; (6) Normal range of blood count, heart, liver, and kidney function; (7) Sign the informed consent form.

排除标准:

(1)5年内患有其他肿瘤史; (2)EGFR 20外显子突变者; (3)预计生存期<3个月者; (4)严重心肝肾疾病患者; (5)妊娠或哺乳期妇女; (6)精神障碍者; (7)正在参加其它药物试验者。

Exclusion criteria:

(1) Other tumor history within 5 years; (2) EGFR detected sensitive type (20 exon mutations); (3) Expected survival< 3 months; (4) Patients with severe liver, liver, and kidney diseases; (5)Patients during pregnancy or lactation; (6) Persons with a history of mental illness. (7) Patients who are currently participating in other drug trials.

研究实施时间:

Study execute time:

From 2021-10-01 00:00:00 To 2024-09-30 00:00:00  

征募观察对象时间:

Recruiting time:

From 2022-06-02 00:00:00 To 2024-09-30 00:00:00  

干预措施:

Interventions:

组别:

试验组

样本量:

60

Group:

experimental group

Sample size:

干预措施:

肺岩宁方+ 吉非替尼

干预措施代码:

Intervention:

Feiyanning prescription + Gefitinib

Intervention code:

组别:

对照组

样本量:

60

Group:

control group

Sample size:

干预措施:

吉非替尼 + 安慰剂

干预措施代码:

Intervention:

Gefitinib + placebo

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):

徐汇区 

Country:

China 

Province:

Shanghai 

City:

Xuhui District 

单位(医院):

上海中医药大学附属龙华医院 

单位级别:

三级甲等 

Institution
hospital:

Longhua Hospital, Shanghai University of Traditional 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:

疾病控制时间

指标类型:

次要指标

Outcome:

duration of disease control

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

生存质量

指标类型:

次要指标

Outcome:

The quality of life

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

中医临床证候症状

指标类型:

次要指标

Outcome:

TCM clinical syndromes and symptoms

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血清肿瘤标志物

指标类型:

次要指标

Outcome:

Serum tumor markers

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

淋巴细胞亚型

指标类型:

次要指标

Outcome:

Lymphocyte subtype

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

安全性指标

指标类型:

次要指标

Outcome:

Safety index

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:

结束

/Completed

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 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):

由随机中心人员,依照完全随机的方法,运用SPSS 22.0给定种子,按1:1的比例生成随机数字表。

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

According to the completely random method, SPSS 22.0 seed was used to generate the random number table at the ratio of 1:1 by random center staff.

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:

双盲,对所有参与试验的人员(包括受试者和研究人员)设盲

Blinding:

Double blind, blinding all participants in the trial (including subjects and researchers)

是否共享原始数据:

IPD sharing

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):

2025年3月1日,Resman

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

On March 1st, 2025, Resman

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:

 2024-12-13 15:26:12