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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: |
ChiCTR2400088169 |
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最近更新日期: Date of Last Refreshed on: |
2024-08-13 09:20:24 |
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注册时间: Date of Registration: |
2024-08-13 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
低剂量阿糖胞苷联合维奈克拉和阿扎胞苷(VA)对照VA方案诱导治疗老年急性髓系白血病的随机对照研究 |
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Public title: |
Comparison of efficacy and safety between Venetoclax, azacitidine (VA) and VA combined with low-dose cytarabine (VAA) in treatment-naive, elderly patients with acute myeloid leukemia: a randomized controlled trial |
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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: |
低剂量阿糖胞苷联合维奈克拉和阿扎胞苷(VA)对照VA方案诱导治疗老年急性髓系白血病的随机对照研究 |
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Scientific title: |
Comparison of efficacy and safety between Venetoclax, azacitidine (VA) and VA combined with low-dose cytarabine (VAA) in treatment-naive, elderly patients with acute myeloid leukemia: a randomized controlled trial |
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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: |
韩潇 |
研究负责人: |
文钦 |
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Applicant: |
Han Xiao |
Study leader: |
Wen Qin |
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申请注册联系人电话: Applicant telephone: |
+86 181 8959 6376 |
研究负责人电话:
Study leader's |
+86 136 5833 7056 |
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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: |
zxiao2@126.com |
研究负责人电子邮件: Study leader's E-mail: |
qiqi105@sina.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: |
重庆市沙坪坝区新桥正街83号 |
研究负责人通讯地址: |
重庆市沙坪坝区新桥正街83号 |
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Applicant address: |
No.83 Xinqiao main Street, Shapingba District, Chngqing |
Study leader's address: |
No.83 Xinqiao main Street, Shapingba District, Chngqing |
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申请注册联系人邮政编码: Applicant postcode: |
400037 |
研究负责人邮政编码: Study leader's postcode: |
400037 |
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申请人所在单位: |
陆军军医大学第二附属医院 |
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Applicant's institution: |
Second Affiliated Hospital, Army Medical University |
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研究负责人所在单位: |
陆军军医大学第二附属医院 |
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Affiliation of the Leader: |
Second Affiliated Hospital, Army Medical University |
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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: |
2023-研第115-02 |
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: |
陆军军医大学第二附属医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of second Affiliated Hospital of Army Medical University,PLA |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-10-25 00:00:00 | ||
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伦理委员会联系人: |
刘丹 |
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Contact Name of the ethic committee: |
Dan Liu |
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伦理委员会联系地址: |
重庆市沙坪坝区新桥正街83号 |
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Contact Address of the ethic committee: |
No.83, Xinqiao main street, Shapingba District, Chongqing |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 68755422 |
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: |
陆军军医大学第二附属医院 |
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Primary sponsor: |
Second Affiliated Hospital, Army Medical University |
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研究实施负责(组长)单位地址: |
重庆市沙坪坝区新桥正街83号 |
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Primary sponsor's address: |
No.83 Xinqiao main Street, Shapingba District |
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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: |
患者支付医疗费用 |
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Source(s) of funding: |
Patients pay for medical care |
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研究疾病: |
急性髓系白血病 |
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Target disease: |
Acute meyloid leukemia |
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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: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
I期临床试验 | ||||||||||||||||||||||
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Study phase: |
1 |
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研究设计: |
病例对照研究 |
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Study design: |
Case-Control study |
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研究目的: |
探索低剂量阿糖胞苷联合维奈克拉和阿扎胞苷对照维奈克拉和阿扎胞苷治疗老年急性髓系白血病,为达到更高的缓解率及MRD转阴率提供新手段。 |
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Objectives of Study: |
To explore the role of venetoclax with azacitidine and low-dose cytarabine in the higher remission rate and MRD negative rate for newly diagnosed older adult acute myeloid leukemia, thereby improving the survival rate and prognosis. |
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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.患者充分了解本研究,自愿参加并签署知情同意书(ICF); 2.诊断急性髓系白血病的60-90岁(包括界值)老年患者,性别不限; 3.ECOG评分≤3分,或KPS评分≥90分,或PS评分≤1分; 4.预计生存期>3个月; 5.入组前4周内不得接受放疗,化疗,靶向治疗,造血干细胞移植或任何其他治疗。 |
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Inclusion criteria |
1. The patient fully understands this study and voluntarily participates and signs an Informed Consent Form (ICF); 2. Patients diagnosed with adult acute myeloid leukemia; Elderly patients aged 60 to 90 years (including threshold); No gender limitation; 3. ECOG score ≤ 3 points; or KPS score ≥90 points; or PS score ≤1 points; 4. The expected survival period is>3 months; 5.No radiotherapy, chemotherapy, targeted therapy, hematopoietic stem cell transplantation, or any other treatment should be received within 4 weeks prior to enrollment. |
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排除标准: |
1.<60岁且可接受标准剂量或大剂量化疗的患者; 2.有影响生存的严重心脏疾病或肺功能异常者; 3.合并有活动性第二肿瘤; 4.无法保证完成必须的治疗计划和随访观察的患者; 5.研究者判断,不适宜参加本研究的患者。 |
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Exclusion criteria: |
1. Under 60 years old who can accept standard dose or intensive chemotherapy; 2. Individuals with severe heart disease or abnormal lung function that affects survival; 3. Merge active second tumor; 4. Can not come back for eximination on time; 5. Unsuitable subjects for this study determined by the investigator. |
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研究实施时间: Study execute time: |
从 From 2023-10-31 00:00:00至 To 2026-07-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-11-01 00:00:00 至 To 2026-07-31 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): |
由https://www.sealedenvelope.com/randomisation/ simulation/?CSRFToken=bogus-form-not-submitted# 产生随机编码,试验组及对照组按照1:1比例随机入组,根据随机结果决定分组。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Generate a random code by https://www.sealedenvelope.com/randomisation/ simulation/?CSRFToken=bogus-form-not-submitted# , and the experimental group and control group are randomly assigned in a 1:1 ratio. Grouping is determined based on the random results. |
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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 |
否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): |
原始数据将在临床试验结束后的6个月内通过公共管理平台向公众开放(www.medresman.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): |
The raw data will open to the public with public management platform in the 6 months after clinical trials finished(www.medresman.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: |
用病例记录表记录数据,并用电子采集和管理系统进行数据管理 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
The data were recorded by Case Record Form,(CRF) and managed by 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 |