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注册号: Registration number: |
ChiCTR2300073724 |
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最近更新日期: Date of Last Refreshed on: |
2023-09-14 12:53:14 |
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注册时间: Date of Registration: |
2023-07-19 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: |
载药微球经动脉化疗栓塞术(DEB-TACE)序贯肝动脉灌注化疗(HAIC)治疗不可切除大肝癌(>5cm)患者的疗效和安全性:一项前瞻性、IIB期、单臂研究 |
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Public title: |
Efficacy and safety of transarterial chemoembolization with drug-loaded microspheres (DEB-TACE) sequential hepatic arterial infusion chemotherapy (HAIC) in patients with unresectable large liver cancer (> 5 cm): a prospective, phase IIB, one-arm 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: |
载药微球经动脉化疗栓塞术(DEB-TACE)序贯肝动脉灌注化疗(HAIC)治疗不可切除大肝癌(>5cm)患者的疗效和安全性:一项前瞻性、IIB期、单臂研究 |
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Scientific title: |
Efficacy and safety of transarterial chemoembolization with drug-loaded microspheres (DEB-TACE) sequential hepatic arterial infusion chemotherapy (HAIC) in patients with unresectable large liver cancer (> 5 cm): a prospective, phase IIB, one-arm 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: |
安睿 |
研究负责人: |
安睿 |
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Applicant: |
An Rui |
Study leader: |
An Rui |
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申请注册联系人电话: Applicant telephone: |
+86 182 9201 1352 |
研究负责人电话:
Study leader's |
+86 182 9201 1352 |
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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: |
atczln@163.com |
研究负责人电子邮件: Study leader's E-mail: |
atczln@163.com |
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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: |
陕西省西安市新城区长乐西路127号 |
研究负责人通讯地址: |
陕西省西安市新城区长乐西路127号 |
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Applicant address: |
127 Changle Road West, Xincheng District, Xi'an, Shaanxi |
Study leader's address: |
127 Changle Road West, Xincheng District, Xi'an, Shaanxi |
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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: |
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申请人所在单位: |
空军军医大学附属西京医院 |
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Applicant's institution: |
Xijing Hospital Affiliated to Air Force Medical University |
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研究负责人所在单位: |
空军军医大学附属西京医院 |
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Affiliation of the Leader: |
Xijing Hospital Affiliated to Air Force 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: |
KY20232191-F-1号 |
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: |
中国人民解放军空军军医大学第一附属医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of the First Affiliated Hospital of the PLA Air Force Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-07-11 00:00:00 | ||
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伦理委员会联系人: |
伍晓晓 |
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Contact Name of the ethic committee: |
Wu Xiaoxiao |
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伦理委员会联系地址: |
陕西省西安市新城区长乐西路127号西京医院 |
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Contact Address of the ethic committee: |
127 Changle Road West, Xincheng District, Xi'an, Shaanxi |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 29 8477 1794 |
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: |
空军军医大学附属西京医院 |
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Primary sponsor: |
Xijing Hospital Affiliated to Air Force Medical University |
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研究实施负责(组长)单位地址: |
陕西省西安市新城区长乐西路127号 |
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Primary sponsor's address: |
127 Changle Road West, Xincheng District, Xi'an, Shaanxi |
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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: |
无 |
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Source(s) of funding: |
N/A |
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研究疾病: |
肝癌 |
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Target disease: |
HCC |
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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: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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研究设计: |
单臂 |
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Study design: |
Single arm |
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研究目的: |
探究载药微球经动脉化疗栓塞术(DEB-TACE)序贯肝动脉灌注化疗(HAIC)治疗不可切除大肝癌(>5cm)患者的疗效和安全性 |
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Objectives of Study: |
To explore the efficacy and safety of transarterial chemoembolization with drug loaded microspheres (DEB-TACE) followed by hepatic arterial infusion chemotherapy (HAIC) for patients with unresectable large liver cancer (> 5 cm). |
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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.伴有门静脉主干或同时累及双侧门静脉一级分支的癌栓且无主要流出道; 2.弥漫型肝癌患者; 3.肝功能失代偿者,包括:大量腹水、食道胃静脉曲张出血、肝性脑病; 4.器官(心、肾)功能不全,无法耐受TACE或HAIC治疗者; 5.有其他恶性肿瘤病史; 6.患有需要系统性治疗的活动性感染(包括结核病),HCV或HBV除外; 7.接受过同种异体组织/实体器官移植的受试者; 8.有HIV病史者; 9.30天内有胃肠道出血者,或合并有≥3级胃肠道或非胃肠道瘘; 10.当前正在参与或先前参与过试验用药物研究,或者在研究药物首次给药前4周内使用过试验性器械;有可能干扰试验结果、妨碍受试者全程参与研究的疾病史或疾病证据、治疗或实验室值异常,或研究者认为参加研究不符合受试者的最大获益。 |
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Exclusion criteria: |
1. Cancer thrombus accompanied by main portal vein or involving primary branch of bilateral portal vein and no major outflow tract; 2. Patients with diffuse liver cancer; 3. Hepatic decompensation, including: massive ascites, esophageal and gastric variceal bleeding, hepatic encephalopathy; 4. Organ (heart, kidney) dysfunction, unable to tolerate TACE or HAIC treatment; 5. History of other malignant tumors; 6. Have an active infection (including tuberculosis) that requires systematic treatment, other than HCV or HBV; 7. Subjects who have received allogeneic tissue/solid organ transplants; 8. People with HIV history; 9. 30 days of gastrointestinal bleeding, or combined with >= grade 3 gastrointestinal or non-gastrointestinal fistula; 10. Is currently participating in or has previously participated in an investigational drug study, or has used an investigational device within 4 weeks prior to initial dosing of the investigational drug; Medical history or evidence of disease that may interfere with the test results, prevent the subject from fully participating in the study, abnormal treatment or laboratory values, or the investigator believes that participation in the study is not in the subject's best interest. |
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研究实施时间: Study execute time: |
从 From 2023-07-01 00:00:00至 To 2026-07-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-08-01 00:00:00 至 To 2024-06-30 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): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
N/A |
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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: |
N/A |
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Blinding: |
N/A |
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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): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
N/A |
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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: |
数据采集和管理包含病例记录表(Case Record Form, CRF)与epidata软件进行管理。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Data collection and management include case record form (CRF) and epidata software for management. |
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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 |