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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: |
ChiCTR2000039605 |
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最近更新日期: Date of Last Refreshed on: |
2021-02-03 23:05:52 |
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注册时间: Date of Registration: |
2020-11-03 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: |
【辑】刘科宇医师:该研究尚未获得伦理委员会批准,请于批准后再开始纳入参试者,并与我们联系上传批件。 含苯达莫司汀方案一线治疗惰性B细胞非霍奇金淋巴瘤患者随访登记管理 |
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Public title: |
Bendamustine in the treatment of newly diagnosed indolent non-Hodgkin B-cell lymphoma : a real-world 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: |
含苯达莫司汀方案一线治疗惰性B细胞非霍奇金淋巴瘤患者随访登记管理 |
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Scientific title: |
Bendamustine in the treatment of newly diagnosed indolent non-Hodgkin B-cell lymphoma : a real-world 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: |
刘科宇 |
研究负责人: |
马军/朱军 |
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Applicant: |
Keyu Liu |
Study leader: |
Jun Ma/Jun Zhu |
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申请注册联系人电话: Applicant telephone: |
+86 451-84888631 |
研究负责人电话: Study leader's telephone: |
+86 13304518000/10-88196115 |
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申请注册联系人传真 : Applicant Fax: |
+86 451-84883681 |
研究负责人传真: Study leader's fax: |
+86 451-87650339 |
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申请注册联系人电子邮件: Applicant E-mail: |
gesiza@163.com |
研究负责人电子邮件: Study leader's E-mail: |
mjun0322@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: |
黑龙江省哈尔滨市道里区地段街149号 |
研究负责人通讯地址: |
黑龙江省哈尔滨市道里区地段街149号/北京市海淀区阜成路52号 |
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Applicant address: |
149 Diduan Street, Daoli District, Harbin, Heilongjiang, China |
Study leader's address: |
149 Diduan Street, Daoli District, Harbin, Heilongjiang, China/ 52 Fucheng, Haidian District, Beijing, China |
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申请注册联系人邮政编码: Applicant postcode: |
150010 |
研究负责人邮政编码: Study leader's postcode: |
150010 |
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申请人所在单位: |
哈尔滨市第一医院 |
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Applicant's institution: |
Harbin First Hospital |
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研究负责人所在单位: |
哈尔滨市第一医院/ 北京大学肿瘤医院 |
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Affiliation of the Leader: |
Harbin First Hospital/ Peking University Cancer Hospital |
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是否获伦理委员会批准: |
否/No |
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Approved by ethic committee: |
No |
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伦理委员会批件文号: Approved No. of ethic committee: |
伦理委员会批件附件: Approved file of Ethical Committee: |
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批准本研究的伦理委员会名称: |
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Name of the ethic committee: |
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伦理委员会批准日期: Date of approved by ethic committee: |
2013-08-26 00:00:00 |
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伦理委员会联系人: |
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Contact Name of the ethic committee: |
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伦理委员会联系地址: |
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Contact Address of the ethic committee: |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
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: |
哈尔滨血液病肿瘤研究所 /北京大学肿瘤医院 |
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Primary sponsor: |
Harbin First Hospital/ Peking University Cancer Hospital |
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研究实施负责(组长)单位地址: |
黑龙江省哈尔滨市道里区地段街149号/北京市海淀区阜成路52号 |
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Primary sponsor's address: |
149 Diduan Street, Daoli District, Harbin, Heilongjiang, China/ 52 Fucheng, Haidian District, Beijing, 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: |
北京康盟慈善基金会 |
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Source(s) of funding: |
Beijing Health Allicance Charitable Foundation |
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Target disease: |
Indolent non-Hodgkin B-cell lymphoma |
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Target disease code: |
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研究类型: |
观察性研究 |
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Study type: |
Observational 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: |
连续入组 |
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Study design: |
Sequential |
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研究目的: |
描述含苯达莫司汀方案一线治疗惰性B细胞非霍奇金淋巴瘤患者的治疗模式(包括治疗方案,用药剂量,治疗周期数,剂量调整/停药及原因)和治疗结局,分析苯达莫司汀治疗患者的人口学特征和临床特征及其与治疗结局的关系,收集治疗过程中患者出现的不良事件(AE)和严重不良事件(SAE),观察苯达莫司汀用药安全性 |
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Objectives of Study: |
To describe the treatment mode(such as therapeutic regimen, dosage of medicine,treatment cycles,reason of dose adjustment and drug discontinuance) of that bendamustine in the treatment of newly diagnosed indolent non-Hodgkin B-cell lymphoma patients, analyze the demographic characteristics , clinical features and its relationship with treatment outcome, collect adverse events (AE) and serious adverse event (SAE), and probe therapeutic regimens safety. |
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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18~75岁,病理学确诊为CD20+惰性B细胞非霍奇金淋巴瘤的患者,包括滤泡性淋巴瘤1-3a级、淋巴浆细胞淋巴瘤(华氏巨球蛋白血症)、边缘区淋巴瘤、慢性淋巴细胞白血病/小淋巴细胞淋巴瘤; |
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Inclusion criteria |
1. Aged 18-75 years,diagnosed as CD20-positive Indolent non-Hodgkin B-cell lymphoma(containing follicular lymphoma of grade 1-3a, waldenstrom macroglobulinemia, marginal zone lymphoma,chronic lymphocytic leukemia/small lymphocytic lymphoma); |
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排除标准: |
(1)已知对治疗方案中的任何药物过敏或者代谢障碍者; |
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Exclusion criteria: |
1. Patients who are known to be allergic to any drug in the treatment plan or have metabolic disorders; |
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研究实施时间: Study execute time: |
从 From 2020-10-25 00:00:00至 To 2022-09-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2020-10-25 00:00:00 至 To 2021-10-25 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): |
未使用 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Not used |
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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 |
Yes |
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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): |
发表期刊文章 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Publish journal articles |
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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: |
填写病例记录表病进行数据采集并使用EDC系统进行管理 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Fill in case record form to collect data and use EDC system for management |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |