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注册号: Registration number: |
ChiCTR2300075233 |
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最近更新日期: Date of Last Refreshed on: |
2024-01-22 21:58:20 |
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注册时间: Date of Registration: |
2023-08-30 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
PTC指导下的转移性胰腺癌一线精准治疗:一项前瞻性、开放标签、 多中心、非随机对照Ⅱ期研究 |
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Public title: |
First-line precision theatment guided by patient-derived tumor-like cell clusters for metastatic pancreatic cancer: a prospective, open-label, multicenter, non-randomized, phase II study |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
PTC指导下的转移性胰腺癌一线精准治疗:一项前瞻性、开放标签、 多中心、非随机对照Ⅱ期研究 |
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Scientific title: |
First-line precision theatment guided by patient-derived tumor-like cell clusters for metastatic pancreatic cancer: a prospective, open-label, multicenter, non-randomized, phase II study |
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研究课题代号(代码): Study subject ID: |
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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: |
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申请注册联系人: |
王晓盈 |
研究负责人: |
蒋华 |
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Applicant: |
Xiaoying Wang |
Study leader: |
Hua Jiang |
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申请注册联系人电话: Applicant telephone: |
+86 158 5192 2993 |
研究负责人电话:
Study leader's |
+86 180 1585 2711 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
czwxying@126.com |
研究负责人电子邮件: Study leader's E-mail: |
czeyjh@njmu.edu.cn |
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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): |
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申请注册联系人通讯地址: |
江苏省常州市武进区滆湖中路68号 |
研究负责人通讯地址: |
江苏省常州市武进区滆湖中路68号 |
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Applicant address: |
68 Gehu Middle Road, Wujin District, Changzhou, Jiangsu, China |
Study leader's address: |
68 Gehu Middle Road, Wujin District, Changzhou, Jiangsu, China |
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申请注册联系人邮政编码: Applicant postcode: |
212000 |
研究负责人邮政编码: Study leader's postcode: |
212000 |
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申请人所在单位: |
南京医科大学附属常州第二人民医院 |
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Applicant's institution: |
The Affliated Changzhou Second People's Hospital of Nanjing Medical University |
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研究负责人所在单位: |
南京医科大学附属常州第二人民医院 |
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Affiliation of the Leader: |
The Affliated Changzhou Second People's Hospital of Nanjing Medical University |
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是否获伦理委员会批准: |
是 |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
[2023]YLJSA026 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
常州市第二人民医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Changzhou Second People's Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-08-10 00:00:00 | ||
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伦理委员会联系人: |
黄芳 |
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Contact Name of the ethic committee: |
Fang Huang |
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伦理委员会联系地址: |
江苏省常州市武进区滆湖中路68号 |
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Contact Address of the ethic committee: |
68 Gehu Middle Road, Wujin District, Changzhou, Jiangsu, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 137 7562 4815 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
南京医科大学附属常州第二人民医院 |
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Primary sponsor: |
The Affliated Changzhou Second People's Hospital of Nanjing Medical University |
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研究实施负责(组长)单位地址: |
江苏省常州市武进区滆湖中路68号 |
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Primary sponsor's address: |
68 Gehu Middle Road, Wujin District, Changzhou, Jiangsu, China |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
自筹 |
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Source(s) of funding: |
Self-financed |
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研究疾病: |
转移性胰腺癌 |
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Target disease: |
Metastatic pancreatic cancer |
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研究疾病代码: |
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Target disease code: |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
II期临床试验 | ||||||||||||||||||||||
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Study phase: |
2 |
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研究设计: |
非随机对照试验 |
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Study design: |
Non randomized control |
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研究目的: |
评估PTC指导下转移性胰腺癌的一线精准治疗是否优于现有指南推荐治疗。 |
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Objectives of Study: |
To evaluate whether the first-line precision treatment of metastatic pancreatic cancer guided by Patient-derived tumor-like cell clusters (PTC) is better than the treatment recommended by current guidelines. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
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Inclusion criteria |
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排除标准: |
1. 过去5年内患有其他恶性肿瘤,不包括已治愈的皮肤基底细胞癌、宫颈原位癌和甲状腺乳头状癌; 2. 试验期间需要接受择期手术患者; 3. 无法口服吞咽药物,或存在经研究者判断严重影响胃肠道吸收的状况如慢性腹泻、肠梗阻等不合适治疗患者; 4. 妊娠期(妊娠试验阳性)或哺乳期患者; 5. 中枢神经系统转移或脑膜转移; 6. 不可控制的骨转移,或有骨折风险、需要手术、局部放疗的患者; 7. 有活动性感染,需要系统性抗感染治疗患者; 8. 有免疫缺陷病史,包括HIV抗体检测阳性患者; 9. 已知的、活动的自身免疫性疾病患者; 10. 未控制的活动性乙型肝炎患者,有丙型肝炎病毒感染患者(丙肝抗体阳性); 11. 有严重的心脑血管疾病史,包括但不限于:有严重的心律失常、半年内发生急性冠脉综合征、充血性心力衰竭、主动脉夹层、脑卒中、TIA史等; 12. 半年内发生严重出血事件,或存在高出血风险因素如活动性消化道溃疡、肝硬化食管胃底静脉曲张; 13. 药物(包括胰岛素)不能稳定控制的糖尿病患者; 14. 精神或语言障碍,不能交流患者; 15. 同时参加另一项临床试验患者; 16. 已知肿瘤存在MSI-H/dMMR; 17. 研究者认为受试者存在其他严重的系统性疾病、或其他情况而不适应参加本试验者。 |
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Exclusion criteria: |
1. Other malignancies in the past 5 years, excluding cured basal cell carcinoma of the skin, carcinoma in situ of the cervix, and papillary carcinoma of the thyroid; 2. Patients requiring elective surgery during the trial; 3. Patients who are unable to swallow drugs orally or have conditions that researchers judge to seriously affect gastrointestinal absorption, such as chronic diarrhea and intestinal obstruction; 4. Pregnant (pregnancy test positive) or breastfeeding patients; 5. Central nervous system metastasis or meningeal metastasis; 6. Uncontrolled bone metastases, or patients at risk of fracture, requiring surgery or local radiotherapy; 7. Patients with active infection requiring systemic anti-infection treatment; 8. Have a history of immunodeficiency, including HIV antibody test positive patients; 9. Patients with known, active autoimmune diseases; 10. Uncontrolled active hepatitis B patients with hepatitis C virus infection (hepatitis C antibody positive); 11. History of severe cardiovascular and cerebrovascular diseases, including but not limited to: severe arrhythmia, acute coronary syndrome within six months, congestive heart failure, aortic dissection, stroke, TIA, etc; 12. Severe bleeding events within six months, or high blood risk factors such as active gastrointestinal ulcers, cirrhosis of the esophagus and gastric varices; 13. Patients with diabetes who cannot be stably controlled by medication (including insulin); 14. Patients with mental or language disorders who cannot communicate; 15. Patients participating in another clinical trial at the same time; 16. Patients with MSI-H/dMMR; 17. According to researcher's consideration, patients with other serious systemic diseases or other conditions that are not suitable for participation. |
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研究实施时间: Study execute time: |
从 From 2023-09-01 00:00:00至 To 2025-09-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-09-01 00:00:00 至 To 2025-03-01 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
非随机 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Not randomly |
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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 |
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盲法: |
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Blinding: |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
否No |
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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): |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
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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: |
病例记录表 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Record Form, CRF |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |