静脉使用维生素C联合射频热疗对肺癌患者的安全性及有效性的临床研究

注册号:

Registration number:

ChiCTR-IIR-16007801 

最近更新日期:

Date of Last Refreshed on:

2016-01-20 20:49:02 

注册时间:

Date of Registration:

2016-01-20 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

静脉使用维生素C联合射频热疗对肺癌患者的安全性及有效性的临床研究

Public title:

Safety and Efficacy of Vitamin C Infusion in Combination With Local mEHT to Treat Non Small Cell Lung Cancer

注册题目简写:

English Acronym:

研究课题的正式科学名称:

静脉使用维生素C联合射频热疗对非小细胞肺癌患者的安全性及有效性的I/II期临床试验研究

Scientific title:

Phase I/II Study of Vitamin C Infusion in Combination With Local mEHT on Non Small Cell Lung Cancer Patients

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:

区俊文 

研究负责人:

区俊文 

Applicant:

Ou Junwen 

Study leader:

Ou Junwen 

申请注册联系人电话:

Applicant telephone:

+86 13556021810

研究负责人电话:

Study leader's
telephone:

+86 13556021810

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:

Oujunwen66@163.com

研究负责人电子邮件:

Study leader's E-mail:

Oujunwen66@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:

中国广东省广州市番禺区鸿福路3号

研究负责人通讯地址:

中国广东省广州市番禺区鸿福路3号

Applicant address:

3 Hongfu road, Panyu Districg, Guangzhou, Guangdong, China

Study leader's address:

3 Hongfu road, Panyu Districg, Guangzhou, Guangdong, 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:

广州中医药大学祈福医院

Applicant's institution:

CLIFFORD HOSPITAL

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:

2/2015-10

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:

广州中医药大学祈福医院医学伦理委员会

Name of the ethic committee:

CLIFFORD Hospital Medical Ethics Committee

伦理委员会批准日期:

Date of approved by ethic committee:

2013-08-26 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:

广州中医药大学祈福医院

Primary sponsor:

CLIFFORD HOSPITAL

研究实施负责(组长)单位地址:

中国广东省广州市番禺区鸿福路3号

Primary sponsor's address:

3 Hongfu road, Panyu Districg, Guangzhou, Guangdong, 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):

广东

市(区县):

广州

Country:

China

Province:

Guangdong

City:

Guangzhou

单位(医院):

广州中医药大学祈福医院

具体地址:

中国广东省广州市番禺区鸿福路3号,邮编511495

Institution
hospital:

Clifford Hospital

Address:

3 Hongfu road, Panyu Districg, Guangzhou, Guangdong, China

经费或物资来源:

广州中医药大学祈福医院

Source(s) of funding:

CLIFFORD HOSPITAL

研究疾病:

非小细胞肺癌  

Target disease:

non small cell lung cancer

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:

I期+II期 

Study phase:

1-2

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

本研究的目的是观察药理浓度下维生素C联合局部热疗对非小细胞肺癌患者癌灶大小、生存质量、免疫功能及生存期的影响。  

Objectives of Study:

This trial studies efficacy and safety of combination of vitamin C infusion with modulated electro-hyperthermia (mEHT) in treatment of non small cell lung cancer patients.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

Inclusion criteria

排除标准:

肺部癌转移、不是非小细胞肺癌的患者。
G6PD缺乏患者。
对VitC过敏的患者。
无法接受mEHT仪器治疗的患者。
治疗区域戴有金属装置的患者。
戴有心脏起搏器等电子设备的患者。
治疗区域有热感觉神经或者其他感觉组织的损伤。
影响生存时间的其他病症,如充血性心力衰竭,不稳定性心绞痛,心肌梗塞(近6周内),不受控高血糖(>300mg/dL),慢性活动性肝炎或肝硬化。
肾功能受损患者(血清肌酐含量>1.3mg/dl),无尿草酸。
长期血液透析。
铁过量(铁蛋白>500ng/ml)。
诊断为Wilson’s病。
肝功能损伤患者:胆道堵塞或者血胆红素2.0;肝功能测试高于1.5倍正常参考值(ALT>63,AST>95)。
非常低的血白细胞量(<1.5 x 10(9)/L),粒细胞缺乏(< 0.5 x 10(9)/L),严重贫血。
妊娠或哺乳期妇女。
吸烟患者。
影响试验进行及知情同意书填写的精神与心理障碍的患者。

Exclusion criteria:

1. Lung metastasis/not primary non small cell lung cancer;
2. Glucose-6-phosphate dehydrogenase deficiency (G6PD);
3. Vitamin C allergy;
4. Impossibility to place the patient into the mEHT machine;
5. Metallic implants or replacements in the treatment area;
6. Electronic implanted devices anywhere;
7. Missing or damaged heat-sense nerves or other field-sensitive issues in the treatment area;
8. Co-morbid conditions that affect survival: end stage congestive heart failure, unstable angina, myocardial infarction (within the past 6 weeks), and uncontrolled blood sugars of greater than 300 mg/dL, known chronic active hepatitis or cirrhosis;
9. Renal insufficiency as evidenced by serum creatinine of >=1.3mg/dl or evidence of oxalosis by urinalysis;
10. Chronic hemodialysis;
11. Iron overload (a ferritin > 500 ng/ml);
12. Wilson's disease;
13. Compromised liver function with evidence of complete biliary obstruction or have a serum bilirubin of 2.0 or liver function tests (AST > 63, ALT > 95) exceeding 1.5*upper limit of normal;
14. Very low white blood cell count (< 1.5*10^9/L), agranulocytosis (< 0.5*10^9/L) or severe anemia;
15. Pregnant or lactating female;
16. Current tobacco use;
17. Evidence of significant psychiatric disorder by history or examination that would prevent completion of the study or preclude informed consent.

研究实施时间:

Study execute time:

From 2016-01-20 00:00:00 To 2016-12-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2016-01-20 00:00:00 To 2016-07-01 00:00:00

干预措施:

Interventions:

组别:

试验组

样本量:

35

Group:

treatment group

Sample size:

干预措施:

静脉维生素C注射

干预措施代码:

Intervention:

vitamin C infusion

Intervention code:

组别:

试验组

样本量:

35

Group:

treatment group

Sample size:

干预措施:

射频热疗

干预措施代码:

Intervention:

Electro-Hyperthermia

Intervention code:

组别:

试验组

样本量:

35

Group:

treatment group

Sample size:

干预措施:

营养咨询与生活方式宣教

干预措施代码:

Intervention:

Lifestyle counseling

Intervention code:

组别:

对照组

样本量:

35

Group:

control group

Sample size:

干预措施:

营养咨询与生活方式宣教

干预措施代码:

Intervention:

Lifestyle counseling

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

广州 

市(区县):

 

Country:

China

Province:

Guangzhou

City:

单位(医院):

祈福医院 

单位级别:

三甲医院 

Institution
hospital:

CLIFFORD HOSPITAL

Level of the institution:

Tertiary A hospital

测量指标:

Outcomes:

指标中文名:

维生素C联合局部热疗治疗的安全性

指标类型:

主要指标

Outcome:

Safety of vitamin C infusion in combination with oncothermia on NSCLC patients

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

抗肿瘤效果

指标类型:

次要指标

Outcome:

Anti-Tumor Response

Type:

Secondary indicator

测量时间点:

测量方法:

试验结束后即接受CEA,CA199 CA125,CA153,NSE,SCC肿瘤指标检测;试验前及试验后三个月进行CT扫描。

Measure time point of outcome:

Measure method:

Tumor markers such as CEA,CA199 CA125,CA153,NSE,SCC will be evaluated at baseline and immediately after completion of treatment. CT scan will be performed at baseline and 3 months on completion of treatment to measure the size of the tumor

指标中文名:

血液中CD4+,CD8+指标

指标类型:

次要指标

Outcome:

Levels of CD4+,CD8+

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

免疫组化

指标类型:

次要指标

Outcome:

Biomarkers of inflammation

Type:

Secondary indicator

测量时间点:

测量方法:

免疫组化包括CRP,TNF, IL-6, IL-2 等指标的检测。

Measure time point of outcome:

Measure method:

Inflamation biomarkers such as CRP,TNF, IL-6, IL-2 will be tested in the lab

指标中文名:

生活质量的改变(EORTC QLQ-C30)

指标类型:

次要指标

Outcome:

Health Related Quality of Life (EORTC QLQ-C30)

Type:

Secondary indicator

测量时间点:

测量方法:

通过EORTC QLQ-C30的问卷调查。

Measure time point of outcome:

Measure method:

EORTC QLQ-C30

指标中文名:

生存时间

指标类型:

次要指标

Outcome:

Survival time

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:

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:

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):

试验执行者把受试者通过完全随机化分组等分为两组:试验组(35人)、对照组(35人),进行单盲试验。

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

Study performer,using simple randomization design, divide the objects into two groups:treatment group(n=35), control group(n=35). It was single-blinded study.

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):

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

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:

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

数据与安全监察委员会:

Data and Safety Monitoring Committee:

注册人:

Name of Registration:

 2016-01-20 20:49:02