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注册号: Registration number: |
ChiCTR-OPC-17011137 |
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最近更新日期: Date of Last Refreshed on: |
2017-04-13 11:53:26 |
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注册时间: Date of Registration: |
2017-04-13 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: |
一项复方黄黛片联合全反式维甲酸(ATRA)治疗老年骨髓增生异常综合征难治性贫血伴原始细胞增多(MDS-RAEB)的前瞻性、开放标签性、多中心临床研究 |
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Public title: |
An open-label, multicenter, prospective study for Realgar-Indigo naturalis Formula(RIF) combined with All-Trans-Retinoic Acid(ATRA) in old subjects with Myelodysplastic Syndromes-Refractory Anemia with Excess Blasts (MDS-RAEB) |
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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: |
一项复方黄黛片联合全反式维甲酸(ATRA)治疗老年骨髓增生异常综合征难治性贫血伴原始细胞增多(MDS-RAEB)的前瞻性、开放标签性、多中心临床研究 |
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Scientific title: |
An open-label, multicenter, prospective study for Realgar-Indigo naturalis Formula(RIF) combined with All-Trans-Retinoic Acid(ATRA) in old subjects with Myelodysplastic Syndromes-Refractory Anemia with Excess Blasts (MDS-RAEB) |
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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: |
徐泽锋 |
研究负责人: |
肖志坚 |
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Applicant: |
Zefeng Xu |
Study leader: |
Zhijian Xiao |
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申请注册联系人电话: Applicant telephone: |
+86 22 23909046 |
研究负责人电话:
Study leader's |
+86 22 23909184 |
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申请注册联系人传真 : Applicant Fax: |
+86 22 27313013 |
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: |
gbxzf@163.com |
研究负责人电子邮件: Study leader's E-mail: |
zjxiao@medmail.com.cn |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
www.chinablood.com.cn |
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: |
天津市南京路288号 |
研究负责人通讯地址: |
天津市南京路288号 |
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Applicant address: |
288 Nanjing Road, Tianjin, China |
Study leader's address: |
288 Nanjing Road, 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 and Blood Diseases Hospital, Chinese Academy of Medical Sciences |
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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 and Blood Diseases Hospital, Chinese Academy of Medical Sciences |
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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: |
IIT2017002-EC-1 |
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: |
2017-04-06 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 and Blood Diseases Hospital, Chinese Academy of Medical Sciences |
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研究实施负责(组长)单位地址: |
天津市南京路288号 |
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Primary sponsor's address: |
288 Nanjing Road, 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: |
中国医学科学院血液病医院(血液学研究所) |
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Source(s) of funding: |
Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences |
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研究疾病: |
骨髓增生异常综合征 |
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Target disease: |
Myelodysplastic Syndromes |
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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: |
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: |
研究主要目的是评价复方黄黛片联合ATRA治疗老年骨髓增生异常综合征RAEB(MDS-RAEB)患者的近期疗效和安全性。研究的主要疗效指标是评价复方黄黛片联合ATRA给药方案的总体反应率(ORR=CR+PR+HI)。次要疗效指标是评价骨髓完全缓解率(mCR)、细胞遗传学缓解率、输血需求情况、住院情况、安全性和生活质量。 |
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Objectives of Study: |
The study objectives are to assess the safety and tolerability of Realgar-Indigo naturalis Formula(RIF) combined with All-Trans-Retinoic Acid(ATRA) in old subjects with Myelodysplastic syndrome (MDS-RAEB), as well as the overall response rate according to the IWG 2006 response criteria, hematologic improvement, cytogenetic response rates, transfusion requirements, the hospitalizations and Quality of life(QOL). |
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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.年龄<60岁;2.30天内参加过其他的临床试验者;3.有肿瘤病史并且在过去的3年内接受过任何针对此肿瘤的治疗,但除去浅表性膀胱癌、皮肤的基底层细胞或鳞状上皮细胞癌、宫颈上皮内癌变(CIN)或前列腺上皮内癌变(PIN);4.有活动性的病毒或细菌感染,且未能用适当的抗感染治疗进行控制;5.已知艾滋病毒或活动性丙肝病毒的血清学反应为阳性;6.有未控制的心脏疾病的患者;7.患有精神疾患或其他病情而不能配合研究治疗和监测的要求;8.骨髓空抽;9.已知对砷剂或全反式维甲酸中任一成分过敏者;10.曾接受过砷剂或维甲酸治疗,或者在过去1年内接受过造血干细胞移植。 |
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Exclusion criteria: |
Potential subjects who meet any of the following criteria will be excluded from participating in the study: |
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研究实施时间: Study execute time: |
从 From 2017-05-01 00:00:00至 To 2018-06-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2017-05-01 00:00:00 至 To 2018-06-30 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): |
NO |
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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 |
是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): |
中国医学科学院血液病医院(血液学研究所) |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Institute of Hematology and Blood Diseases Hospital , Chinese Academy of Medical Sciences |
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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(血液学研究所) |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Institute of Hematology and Blood Diseases Hospital , Chinese Academy of Medical Sciences |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |