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注册号: Registration number: |
ChiCTR1800018710 |
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最近更新日期: Date of Last Refreshed on: |
2018-10-04 21:46:20 |
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注册时间: Date of Registration: |
2018-10-04 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: |
白蛋白紫杉醇、吉西他滨联合大剂量地塞米松(GAD方案)治疗复发/难治性外周T细胞淋巴瘤的II期临床研究 |
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Public title: |
Gemcitabine, Nab-paclitaxel, and Dexamethasone in Patients With Recurrent/refractory peripheral T cell lymphoma |
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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: |
白蛋白紫杉醇、吉西他滨联合大剂量地塞米松(GAD方案)治疗复发/难治性外周T细胞淋巴瘤的II期临床研究 |
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Scientific title: |
Gemcitabine, Nab-paclitaxel, and Dexamethasone in Patients With Recurrent/refractory peripheral T cell lymphoma |
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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: |
王钊 |
研究负责人: |
林桐榆 |
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Applicant: |
Zhao WANG |
Study leader: |
Tongyu LIN |
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申请注册联系人电话: Applicant telephone: |
+86 13632427963 |
研究负责人电话:
Study leader's |
+86 13926400320 |
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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: |
wangzhao@sysucc.org.cn |
研究负责人电子邮件: Study leader's E-mail: |
tongyulin@hotmail.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: |
广东省广州市东风东路651号 |
研究负责人通讯地址: |
广东省广州市东风东路651号 |
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Applicant address: |
651 East Dongfeng Road, Guangzhou, Guangdong, China |
Study leader's address: |
651 East Dongfeng Road, Guangzhou, Guangdong, China |
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申请注册联系人邮政编码: Applicant postcode: |
510000 |
研究负责人邮政编码: Study leader's postcode: |
510000 |
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申请人所在单位: |
中山大学肿瘤防治中心 |
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Applicant's institution: |
Sun Yat-sen University Cancer Center |
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研究负责人所在单位: |
中山大学肿瘤防治中心 |
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Affiliation of the Leader: |
Sun Yat-sen University Cancer 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: |
B2018-072-01 |
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: |
中山大学肿瘤防治中心伦理委员会 |
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Name of the ethic committee: |
The Ethics committee of Sun Yat-sen University Cancer Center |
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伦理委员会批准日期: Date of approved by ethic committee: |
2018-09-19 00:00:00 | ||
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伦理委员会联系人: |
彭望清 |
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Contact Name of the ethic committee: |
Wangqing PENG |
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伦理委员会联系地址: |
广东省广州市东风东路651号 |
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Contact Address of the ethic committee: |
651 East Dongfeng Road, Guangzhou, Guangdong, China |
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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: |
中山大学肿瘤防治中心 |
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Primary sponsor: |
Sun Yat-sen University Cancer Center |
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研究实施负责(组长)单位地址: |
广东省广州市东风东路651号 |
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Primary sponsor's address: |
651 East Dongfeng Road, Guangzhou, Guangdong, 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: |
中山大学临床医学研究5010计划 |
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Source(s) of funding: |
The foundation of 5010 Clinical Trials of Sun Yat-sen University |
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研究疾病: |
外周T细胞淋巴瘤 |
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Target disease: |
peripheral T cell lymphoma |
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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: |
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: |
评估白蛋白紫杉醇、吉西他滨联合大剂量地塞米松治疗复发/难治性外周T细胞淋巴瘤的疗效 |
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Objectives of Study: |
To evaluate the efficacy and safety of albumin paclitaxel and gemcitabine combined with high dose dexamethasone in the treatment of recurrent/refractory peripheral T cell lymphoma |
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药物成份或治疗方案详述: |
白蛋白紫杉醇、吉西他滨联合大剂量地塞米松(白蛋白结合型紫杉醇 175 mg/m2,D1+ 吉西他滨 1000 mg/m2,D1+地塞米松20mg/m2,D1-3),14天化疗1次(半程),28天1疗程,共4-6程 |
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Description for medicine or protocol of treatment in detail: |
albumin paclitaxel 175mg/m2,d1,d15 gemcitabine 1000mg/m2,d1,d15 dexamethasone 20mg/m2,d1-d3,d15-d17 Every 4 weeks, a total of 4-6 courses |
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纳入标准: |
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Inclusion criteria |
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排除标准: |
1)转化型淋巴瘤 |
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Exclusion criteria: |
Transformed lymphoma; Participated in other clinical trials in the last 3 months; There is a history of other malignancies secondary to lymphoma, or secondary lymphoma after chemotherapy or radiotherapy,or central invasion of lymphoma; Abnormal laboratory tests: ANC<1.0×10^9/L, HGB<80g/L, PLT<90×10^9/L, ALT >3ULN,Cr>2ULN;active infections, decompensated heart failure, dilated cardiomyopathy that require systemic antibiotic or antiviral therapy, coronary heart disease with depressed ST segment and myocardial infarction, severe organic disease and severe mental disease that have occurred in the last 6 months; Pregnant and lactating women;Treatment for lymphoma was performed within 30 days before enrollment. |
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研究实施时间: Study execute time: |
从 From 2018-10-01 00:00:00至 To 2022-09-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2018-10-01 00:00:00 至 To 2020-09-30 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: |
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,无随机方法 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Non-random study, no random method |
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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: |
N/A |
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Blinding: |
N/A |
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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): |
RDD http://www.researchdata.org.cn/ |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
RDD http://www.researchdata.org.cn/ |
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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 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Record on Case Record Form, CRF |
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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 |