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注册号: Registration number: |
ChiCTR2300067367 |
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最近更新日期: Date of Last Refreshed on: |
2023-05-11 21:44:46 |
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注册时间: Date of Registration: |
2023-01-05 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: |
碳离子光子混合射线并同步化疗治疗进展期食管癌前瞻性Ⅱ期临床研究 |
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Public title: |
A prospective phase II clinical study on locally advanced esophageal cancer treated with concurrent chemotherapy and mixed radiotherapy (carbon ion plus photon radiation) |
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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: |
碳离子光子混合射线并同步化疗治疗进展期食管癌前瞻性Ⅱ期临床研究 |
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Scientific title: |
A prospective phase II clinical study on locally advanced esophageal cancer treated with concurrent chemotherapy and mixed radiotherapy (carbon ion plus photon radiation) |
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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: |
张一贺 |
研究负责人: |
张雁山 |
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Applicant: |
Zhang Yihe |
Study leader: |
Zhang Yanshan |
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申请注册联系人电话: Applicant telephone: |
+86 139 9350 8641 |
研究负责人电话:
Study leader's |
+86 138 3051 0999 |
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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: |
sipen@163.com |
研究负责人电子邮件: Study leader's E-mail: |
13830510999@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: |
甘肃省武威市凉州区宣武街16号 |
研究负责人通讯地址: |
甘肃省武威市凉州区宣武街16号 |
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Applicant address: |
16 Xuanwu Street, Liangzhou District, Wuwei, Gansu |
Study leader's address: |
16 Xuanwu Street, Liangzhou District, Wuwei, Gansu |
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申请注册联系人邮政编码: Applicant postcode: |
733000 |
研究负责人邮政编码: Study leader's postcode: |
733000 |
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申请人所在单位: |
甘肃省武威肿瘤医院重离子中心 |
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Applicant's institution: |
Wuwei Tumor Hospital Heavy Ion Center |
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研究负责人所在单位: |
甘肃省武威肿瘤医院重离子中心 |
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Affiliation of the Leader: |
Wuwei Tumor Hospital Heavy Ion Center |
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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: |
2022-伦理审查-17 |
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: |
甘肃省武威肿瘤医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Gansu Wuwei Tumor Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2022-12-23 00:00:00 | ||
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伦理委员会联系人: |
徐中山 |
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Contact Name of the ethic committee: |
Xu Zhongshan |
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伦理委员会联系地址: |
甘肃省武威市凉州区宣武街16号 |
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Contact Address of the ethic committee: |
16 Xuanwu Street, Liangzhou District, Wuwei, Gansu |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 935 6988500 |
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: |
甘肃省武威肿瘤医院重离子中心 |
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Primary sponsor: |
Wuwei Tumor Hospital Heavy Ion Center |
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研究实施负责(组长)单位地址: |
甘肃省武威市凉州区清源镇重离子医院 |
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Primary sponsor's address: |
Qingyuan Town, Liangzhou District, Wuwei, Gansu |
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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: |
None |
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研究疾病: |
食管癌 |
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Target disease: |
esophageal 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: |
单臂 |
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Study design: |
Single arm |
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研究目的: |
使用新的容积调控放射治疗,或本院特有的碳离子,将局部放疗剂量提升至 6600 cGy,期望达到提高局部肿瘤控制率的目的。 |
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Objectives of Study: |
The dose of local radiotheapy was increased to 6600 cGy by using new Volumetric-Modulated Arc Therapy (VMAT) or carbon ion, hoping to achieve the purpose of improving the local control rate of tumor. |
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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. 已有食道气管瘘管或经医师判断极有可能产生食道气管瘘管的病人; 2. 六个月内体重减轻超过 20%; 3. 妊娠 (经血清或者尿β-HCG 检验证实) 或者泌乳期间; 4. 滥用药物或酒精依赖; 5. 艾滋病患者; 6. 伴有未控制的全身的、肺部的或心脏疾病; 7. 伴有使试验方案不能顺利进行的严重合并症,包括没有控制的合并疾病 (肺功能不足,心血管,肺,肝,肾,糖尿病等) ,成瘾和/或精神疾病; 8. 植入心脏起搏器或其他金属假体足以影响放射治疗进行者; 9. 依从性差的患者,包括可能不能完成治疗计划,或不能接受规定的随访和检查; 10. 曾患有其他恶性肿瘤(非恶性黑色素瘤的皮肤癌或者非浸润性宫颈癌除外); 11. 同时接受全身的免疫治疗或者皮质激素治疗; 12. 血肌酐清除率<30ml/分钟; 13. 放射治疗的禁忌症; 14. 在入组本试验之前 30 天内参加过其他药物临床试验; 15. 无民事行为放射治疗的禁忌症能力或者限制民事行为能力; 16. 任何病史,据研究者判断可能干扰试验结果或增加患者风险; 17. 医师认为不适合参加该试验的任何情况; 18. 患者拒绝签署知情同意书。 |
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Exclusion criteria: |
1. Patients who have already had esophageal and tracheal fistulas or have been judged by doctors to be very likely to have esophageal and tracheal fistulas; 2. Weight loss of more than 20% within six months; 3. During pregnancy (confirmed by serum or urine β-HCG test) or during lactation; 4. Drug abuse or alcohol dependence; 5. AIDS patients; 6. With uncontrolled systemic, pulmonary or cardiac disease; 7. Accompanied by serious comorbidities that prevent the trial program from being carried out smoothly, including uncontrolled comorbid diseases (insufficient lung function, cardiovascular, lung, liver, kidney, diabetes, etc.), addiction and/or mental illness; 8. Implantation of a pacemaker or other metal prosthesis is enough to affect the progress of radiation therapy; 9. Patients with poor compliance, including those who may not be able to complete the treatment plan, or cannot accept the prescribed follow-up visits and examinations; 10. Have suffered from other malignant tumors (except non-malignant melanoma skin cancer or non-invasive cervical cancer); 11. Receive systemic immunotherapy or corticosteroid therapy at the same time; 12. Serum creatinine clearance < 30 ml/min; 13. Contraindications to radiation therapy; 14. Participated in other drug clinical trials within 30 days before enrollment in this trial; 15. No contraindication capacity for civil conduct radiotherapy or limited capacity for civil conduct; 16. Any medical history that, according to the investigator's judgment, may interfere with the test results or increase the risk of the patient; 17. Any situation that the doctor thinks is not suitable for participating in the trial; 18. The patient refuses to sign the informed consent. |
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研究实施时间: Study execute time: |
从 From 2022-12-23 00:00:00至 To 2027-12-23 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-01-05 00:00:00 至 To 2027-12-23 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: |
正在进行 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): |
N/A, 非随机临床研究 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
N/A, non-randomized clinical study |
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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): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
NO |
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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: |
采用excel文档数据库进行保存和管理 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Excel document as the repository will be used for management. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |