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注册号: Registration number: |
ChiCTR-OIC-16008402 |
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最近更新日期: Date of Last Refreshed on: |
2016-05-01 09:59:11 |
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注册时间: Date of Registration: |
2016-05-01 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: |
TCD诱导联合TP方案维持治疗初治症状性LPL/WM的前瞻性多中心临床观察 |
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Public title: |
The efficientcy of thalidomide plus cyclophosphamide and dexamethasone following by thalidomide and prednisone maintaince therapy for the newly diagnosed Waldenstr?m macroglobulinemia - a Prospective Multicentre Phase III Trial from China |
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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: |
TCD诱导联合TP方案维持治疗初治症状性淋巴浆细胞淋巴瘤/华氏巨球蛋白血症的前瞻性多中心临床观察 |
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Scientific title: |
The efficientcy of thalidomide plus cyclophosphamide and dexamethasone following by thalidomide and prednisone maintaince therapy for the newly diagnosed Waldenstr?m macroglobulinemia - a Prospective Multicentre Phase III Trial from China |
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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: |
易树华 |
研究负责人: |
易树华 |
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Applicant: |
Shuhua Yi |
Study leader: |
Shuhua Yi |
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申请注册联系人电话: Applicant telephone: |
+86 15900265415 |
研究负责人电话:
Study leader's |
+86 15900265415 |
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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: |
shuhuayilove@163.com |
研究负责人电子邮件: Study leader's E-mail: |
shuhuayilove@163.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
http://www.chinablood.com.cn/ |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
http://www.chinablood.com.cn/ |
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申请注册联系人通讯地址: |
天津市和平区南京路288号 |
研究负责人通讯地址: |
天津市和平区南京路288号 |
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Applicant address: |
288 Nanjing Road, Heping District, Tianjin, China |
Study leader's address: |
288 Nanjing Road, Heping District, Tianjin, China |
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申请注册联系人邮政编码: Applicant postcode: |
300020 |
研究负责人邮政编码: Study leader's postcode: |
300020 |
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申请人所在单位: |
中国医学科学院血液病医院(血液学研究所) |
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Applicant's institution: |
Institute of Hematology Blood Disease Hospital, Chinese Academy of Medical Sciences Peking Union Medical College |
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研究负责人所在单位: |
中国医学科学院血液病医院(血液学研究所) |
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Affiliation of the Leader: |
Institute of Hematology Blood Disease Hospital, Chinese Academy of Medical Sciences Peking Union Medical College |
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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: |
IIT2015004-EC-2 |
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: |
中国医学科学院血液病医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Blood Diseases Hospital, Chinese Academy of Medical Sciences |
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伦理委员会批准日期: Date of approved by ethic committee: |
2016-04-05 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: |
中国医学科学院血液病医院(血液学研究所) |
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Primary sponsor: |
Institute of Hematology Blood Disease Hospital, Chinese Academy of Medical Sciences Peking Union Medical College |
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研究实施负责(组长)单位地址: |
天津市和平区南京路288号 |
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Primary sponsor's address: |
288 Nanjing Road, Heping District, Tianjin, 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: |
国家科技支撑计划 |
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Source(s) of funding: |
State Science Technology Project in China |
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研究疾病: |
淋巴浆细胞淋巴瘤/华氏巨球蛋白血症 |
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Target disease: |
lymphoplasmacytic lymphoma / Waldenstrom macroglobulinemia |
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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: |
观察性研究 |
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Study type: |
Observational study |
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研究所处阶段: |
III期临床试验 | ||||||||||||||||||||||
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Study phase: |
3 |
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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TCD方案诱导治疗后沙利度胺+泼尼松维持对初治症状性LPL/WM患者的有效性 |
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Objectives of Study: |
To valuate the efficientcy of thalidomide plus cyclophosphamide and dexamethasone following by thalidomide and prednisone maintaince therapy for the newly diagnosed Waldenstr?m macroglobulinemia in a prospective multicentre phase III Trial. |
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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) 过去一年内曾确诊或治疗过B-NHL以外的恶性肿瘤(包括活动性中枢神经系统淋巴瘤); |
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Exclusion criteria: |
1. diagnosed with other malignancies outside B-NHL within one year(including active centre neural system lymphoma); |
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研究实施时间: Study execute time: |
从 From 2016-05-01 00:00:00至 To 2019-11-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2016-05-01 00:00:00 至 To 2019-05-01 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: |
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): |
非随机研究 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
non-randomized trail |
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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 |
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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): |
将于试验结束后1年左右公布数据,以文章发表的形式 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
We will publish the primary data one year later after the clinical trail by the publications |
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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: |
中国医学科学院血液病医院淋巴瘤数据库和思派肿瘤数据公司提供的数据库进行数据存储,数据采集为病例扫描记录。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
repository: our own clinical data and the sipai tumor bank data company. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |