ChiCTR2500098024 版本V1.0 版本创建时间2025/02/28 15:26:00 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:

ChiCTR2500098024 

最近更新日期:

Date of Last Refreshed on:

2025-02-28 15:25:51 

注册时间:

Date of Registration:

2025-02-28 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

基于多组学技术探究新型环状RNA circ_0001642促进结直肠癌进展的双重机制研究

Public title:

Dual mechanism study to explore the novel circular RNA circ_0001642 promoting colorectal cancer progression based on multi-omics technology

注册题目简写:

English Acronym:

研究课题的正式科学名称:

基于多组学技术探究新型环状RNA circ_0001642促进结直肠癌进展的双重机制研究

Scientific title:

Dual mechanism study to explore the novel circular RNA circ_0001642 promoting colorectal cancer progression based on multi-omics technology

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:

缪延栋 

研究负责人:

缪延栋 

Applicant:

Yandong Miao 

Study leader:

Yandong Miao 

申请注册联系人电话:

Applicant telephone:

+86 182 9881 0814

研究负责人电话:

Study leader's
telephone:

+86 182 9881 0814

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:

miaoyd_22@bzmc.edu.cn

研究负责人电子邮件:

Study leader's E-mail:

miaoyd_22@bzmc.edu.cn

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:

山东省烟台市牟平区金埠大街717号

研究负责人通讯地址:

山东省烟台市牟平区金埠大街717号

Applicant address:

No.717 Jinbu Street, Muping District, Yantai City, Shandong Province, China

Study leader's address:

No.717 Jinbu Street, Muping District, Yantai City, Shandong 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:

滨州医学院烟台附属医院

Applicant's institution:

Yantai Affiliated Hospital of Binzhou Medical University

研究负责人所在单位:

滨州医学院烟台附属医院

Affiliation of the Leader:

Yantai Affiliated Hospital of Binzhou Medical University

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:

20250220058

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:

滨州医学院烟台附属医院医学伦理委员会

Name of the ethic committee:

Medical Ethics Committee, Yantai Affiliated Hospital, Binzhou Medical College, China

伦理委员会批准日期:

Date of approved by ethic committee:

2025-02-20 00:00:00

伦理委员会联系人:

李贞颖

Contact Name of the ethic committee:

Zhenying Li

伦理委员会联系地址:

滨州医学院烟台附属医院门诊楼五楼西5010室

Contact Address of the ethic committee:

Room 5010, West 5/F, Outpatient Building, Yantai Affiliated Hospital of Binzhou Medical College, Binzhou, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 535 477 0669

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:

滨州医学院烟台附属医院

Primary sponsor:

Yantai Affiliated Hospital of Binzhou Medical University

研究实施负责(组长)单位地址:

山东省烟台市牟平区金埠大街717号

Primary sponsor's address:

No.717 Jinbu Street, Muping District, Yantai City, Shandong 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):

山东

市(区县):

Country:

China

Province:

Shandong

City:

单位(医院):

滨州医学院烟台附属医院

具体地址:

山东省烟台市牟平区金埠大街717号

Institution
hospital:

Yantai Affiliated Hospital of Binzhou Medical University

Address:

No.717 Jinbu Street, Muping District, Yantai City, Shandong Province, China

经费或物资来源:

滨州医学院烟台附属医院科技计划项目

Source(s) of funding:

Science and Technology Program of Yantai Affiliated Hospital of Binzhou Medical College

研究疾病:

结直肠癌  

Target disease:

Colorectal 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:

连续入组 

Study design:

Sequential 

研究目的:

探究hsa_circ_0001642、hsa-miR-193a-5p、SPHK1用于结直肠癌诊断和治疗的临床意义  

Objectives of Study:

Exploring the clinical significance of hsa_circ_0001642, hsa-miR-193a-5p, and SPHK1 for colorectal cancer diagnosis and treatment

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) 年龄 >=18 岁,确诊为结直肠腺癌(依据术后病理或活检病理),临床分期为 I-IV 期; 2) 前瞻性研究(2025.01-2027.12)需签署知情同意书,自愿提供肿瘤组织、癌旁组织及外周血液样本; 3) 回顾性队列(2019.01-2023.12)需有完整的临床资料及随访记录(包括确诊日期、治疗方案、生存状态等); 4) 未接受过放化疗或靶向治疗(术前新辅助治疗患者可纳入); 5) 可配合完成长期随访(针对回顾性分析)。

Inclusion criteria

1) Age >=18 years, confirmed diagnosis of colorectal adenocarcinoma (based on postoperative pathology or biopsy pathology), clinical stage I-IV; 2) Prospective study (2025.01-2027.12) requires signed informed consent and voluntary provision of tumor tissue, paracancerous tissue and peripheral blood samples; 3) Retrospective cohort (2019.01-2023.12) requires complete clinical data and follow-up records (including date of diagnosis, treatment regimen, survival status, etc.); 4) Have not received radiotherapy or targeted therapy (preoperative neoadjuvant therapy patients can be included); 5) Can cooperate to complete long-term follow-up (for retrospective analysis).

排除标准:

1) 合并其他恶性肿瘤或全身性免疫疾病; 2) 存在严重肝肾功能不全、心脑血管疾病或其他可能影响生存分析的合并症; 3) 临床资料缺失或随访数据不完整(如失访、联系方式错误等); 4) 病理类型为非腺癌(如神经内分泌瘤、淋巴瘤等); 5) 样本采集过程中发生溶血或组织保存不合格(仅适用于前瞻性研究)。

Exclusion criteria:

1) comorbidity with other malignant tumors or systemic immune disorders; 2) Presence of severe hepatic or renal insufficiency, cardiovascular or cerebrovascular disease or other comorbidities that may affect the survival analysis; 3) Missing clinical information or incomplete follow-up data (e.g., missed visits, incorrect contact information, etc.); 4) Pathological type of non-adenocarcinoma (e.g. neuroendocrine tumor, lymphoma, etc.); 5) hemolysis or substandard tissue preservation during sample collection (for prospective studies only).

研究实施时间:

Study execute time:

From 2025-01-01 00:00:00 To 2027-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2025-03-01 00:00:00 To 2026-12-31 00:00:00

干预措施:

Interventions:

组别:

观察组

样本量:

80

Group:

Observation Group

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

组别:

对照组

样本量:

80

Group:

Control 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):

山东 

市(区县):

 

Country:

China

Province:

Shandong

City:

单位(医院):

滨州医学院烟台附属医院 

单位级别:

三甲 

Institution
hospital:

Yantai Affiliated Hospital of Binzhou Medical University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

SPHK1表达水平

指标类型:

主要指标

Outcome:

The expression level of SPHK1

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

hsa_circ_0001642表达水平

指标类型:

主要指标

Outcome:

The expression level of hsa_circ_0001642

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

hsa-miR-193a-5p表达水平

指标类型:

主要指标

Outcome:

The expression level of hsa-miR-193a-5p

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

生存结局指标

指标类型:

主要指标

Outcome:

Survival outcome indicators

Type:

Primary indicator

测量时间点:

测量方法:

总体生存时间、无病生存期、3 年总生存率

Measure time point of outcome:

Measure method:

Overall survival time , disease-free survival, 3- year overall survival rate

指标中文名:

诊断效能指标

指标类型:

主要指标

Outcome:

Diagnostic effectiveness indicators

Type:

Primary indicator

测量时间点:

测量方法:

ROC 曲线下面积、灵敏度、特异性、阳性预测值

Measure time point of outcome:

Measure method:

Area under ROC curve, sensitivity, specificity, positive predictive value

指标中文名:

临床病理参数相关性

指标类型:

次要指标

Outcome:

Correlation of clinicopathologic parameters

Type:

Secondary indicator

测量时间点:

测量方法:

TNM 分期、肿瘤分化程度、淋巴结转移与生物标志物表达的关系

Measure time point of outcome:

Measure method:

Relationship between TNM staging, degree of tumor differentiation, lymph node metastasis and biomarker expression

指标中文名:

患者生活质量评分

指标类型:

次要指标

Outcome:

Patient quality of life scores

Type:

Secondary indicator

测量时间点:

测量方法:

ECOG 评分或 QLQ-C30 量表

Measure time point of outcome:

Measure method:

ECOG score or QLQ-C30 scale

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:

标本中文名:

结直肠癌组织

组织:

Sample Name:

Colorectal cancer tissue

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 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:

不公开/Private

盲法:

Blinding:

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):

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

None

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:

不涉及

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

None

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2025-02-28 15:25:51