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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2500101688 |
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最近更新日期: Date of Last Refreshed on: |
2025-04-28 15:06:01 |
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注册时间: Date of Registration: |
2025-04-28 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: |
甲磺酸多拉司琼注射液预防含顺铂周疗方案同步放化疗所致恶心呕吐的前瞻性真实世界研究 |
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Public title: |
A prospective real-world study on the prevention of nausea and vomiting caused by concurrent chemoradiotherapy with cisplatin-based weekly regimens by dolasetron mesylate injection |
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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: |
甲磺酸多拉司琼注射液预防含顺铂周疗方案同步放化疗所致恶心呕吐的前瞻性真实世界研究 |
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Scientific title: |
A prospective real-world study on the prevention of nausea and vomiting caused by concurrent chemoradiotherapy with cisplatin-based weekly regimens by dolasetron mesylate injection |
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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: |
霍佳 |
研究负责人: |
张松 |
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Applicant: |
Huo Jia |
Study leader: |
Zhang Song |
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申请注册联系人电话: Applicant telephone: |
+86 135 1371 5525 |
研究负责人电话: Study leader's telephone: |
+86 139 3716 6036 |
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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: |
huojiaabc123@163.com |
研究负责人电子邮件: Study leader's E-mail: |
zhangsong09@126.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: |
河南省郑州市二七区建设东路1号 |
研究负责人通讯地址: |
河南省郑州市二七区建设东路1号 |
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Applicant address: |
No. 1, Jianshe East Road, Erqi District, Zhengzhou City, Henan Province |
Study leader's address: |
No. 1, Jianshe East Road, Erqi District, Zhengzhou City, Henan Province |
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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: |
郑州大学第一附属医院 |
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Applicant's institution: |
First Affiliated Hospital of Zhengzhou University |
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研究负责人所在单位: |
郑州大学第一附属医院 |
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Affiliation of the Leader: |
First Affiliated Hospital of Zhengzhou University |
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是否获伦理委员会批准: |
是/Yes |
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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: |
2025-KY-0288-002 |
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: |
郑州大学第一附属医院临床试验伦理委员会 |
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Name of the ethic committee: |
The Clinical Trial Ethics Committee of the First Affiliated Hospital of Zhengzhou University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-04-03 00:00:00 |
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伦理委员会联系人: |
郑州大学第一附属医院临床试验伦理委员会 |
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Contact Name of the ethic committee: |
The Clinical Trial Ethics Committee of the First Affiliated Hospital of Zhengzhou University |
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伦理委员会联系地址: |
河南省郑州市大学路43号 郑州大学第一附属医院 15B楼2层 210 |
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Contact Address of the ethic committee: |
No. 15B, 2nd Floor, 2nd Affiliated Hospital of Zhengzhou University, 43 University Road, Zhengzhou City, Henan Province |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 371 6629 5219 |
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: |
郑州大学第一附属医院 |
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Primary sponsor: |
First Affiliated Hospital of Zhengzhou University |
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研究实施负责(组长)单位地址: |
河南省郑州市二七区建设东路1号 |
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Primary sponsor's address: |
No. 1, Jianshe East Road, Erqi District, Zhengzhou City, Henan Province |
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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: |
辽宁海思科制药有限公司 |
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Source(s) of funding: |
Liaoning Haisco Pharmaceutical Co., Ltd. |
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Target disease: |
malignancy |
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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: |
评价真实世界中基于甲磺酸多拉司琼注射液的方案预防以顺铂周疗为基础的同步放化疗所致恶心呕吐的有效性和安全性 |
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Objectives of Study: |
Evaluate the efficacy and safety of the regimen based on oral administration of dolasetron mesylate injection in preventing nausea and vomiting caused by concurrent chemoradiotherapy with weekly cisplatin administration in the real world setting |
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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: |
1.年龄≥18岁,性别不限; 2.经病理组织学和/或细胞学检查确诊的恶性实体肿瘤; 3.计划接受第一周期含顺铂周疗方案的同步放化疗,顺铂每周给药一次,放疗每周5 天; 4.美国东部肿瘤协作组(ECOG)体力状态评分≤2; 5.预计生存期≥6个月; 6.受试者能够阅读、理解并完成受试者日记 |
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Inclusion criteria |
1. Age >= 18 years old, gender not limited; 2. Malignant solid tumors diagnosed by pathological histology and/or cytology examination; 3. Planned to receive concurrent chemoradiotherapy with cisplatin-based weekly regimen in the first cycle, cisplatin administered once a week, radiotherapy 5 days a week; 4. Eastern Cooperative Oncology Group (ECOG) performance status score <= 2; 5. Expected survival period >= 6 months; 6. The subjects are able to read, understand and complete the subject diary. |
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排除标准: |
1.对甲磺酸多拉司琼注射液及其辅料过敏者; 2.既往证实QT间期>450 ms,或因QT间期延长服用合并药物或存在QT间期延长或相应心律失常事件的风险因素(心衰、高钾血症、长QT综合症病史或家族史); 3.研究者认为不能入组的其他情况。 |
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Exclusion criteria: |
1. Those who are allergic to dolasetron mesylate injection and its excipients; 2. Those who have been confirmed to have QT interval > 450 ms in the past, or have taken concomitant drugs due to prolonged QT interval, or have risk factors for prolonged QT interval or corresponding arrhythmia events (such as heart failure, hyperkalemia, history of long QT syndrome or family history); 3. Other situations that the investigators consider not eligible for inclusion. |
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研究实施时间: Study execute time: |
从 From 2025-04-03 00:00:00至 To 2026-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2025-05-01 00:00:00 至 To 2026-04-30 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): |
None |
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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: |
不公开/Private |
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盲法: |
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Blinding: |
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是否共享原始数据: IPD sharing |
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): |
None |
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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: |
EDC |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
EDC |
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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 |