|
注册号: Registration number: |
ChiCTR2300072614 |
|
最近更新日期: Date of Last Refreshed on: |
2023-08-08 18:30:10 |
|
注册时间: Date of Registration: |
2023-06-19 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
米托蒽醌脂质体联合依托泊苷、阿糖胞苷、 环磷酰胺(PLMEAC)预处理方案治疗NK/T细胞淋巴瘤和T淋巴母细胞淋巴瘤的单臂、 多中心临床研究 |
|
Public title: |
Mitoxantrone liposome combined with etoposide, cytarabine and cyclophosphamide (PLMEAC) in the treatment of NK/T cell lymphoma and T lymphoblastic lymphoma: A single-arm, multicenter study |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
米托蒽醌脂质体联合依托泊苷、阿糖胞苷、 环磷酰胺(PLMEAC)预处理方案治疗NK/T细胞淋巴瘤和T淋巴母细胞淋巴瘤的单臂、 多中心临床研究 |
|
Scientific title: |
Mitoxantrone liposome combined with etoposide, cytarabine and cyclophosphamide (PLMEAC) in the treatment of NK/T cell lymphoma and T lymphoblastic lymphoma: A single-arm, multicenter study |
|
研究课题代号(代码): Study subject ID: |
|
|
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: |
|
申请注册联系人: |
李佳丽 |
研究负责人: |
高力 |
|
Applicant: |
Li Jiali |
Study leader: |
Gao Li |
|
申请注册联系人电话: Applicant telephone: |
+86 135 2736 0198 |
研究负责人电话:
Study leader's |
+86 132 2868 6076 |
|
申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
||
|
申请注册联系人电子邮件: Applicant E-mail: |
KLL6324@163.com |
研究负责人电子邮件: Study leader's E-mail: |
gaotiantiantiger@163.com |
|
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): |
||
|
申请注册联系人通讯地址: |
重庆市沙坪坝区新桥正街183号 |
研究负责人通讯地址: |
重庆市沙坪坝区新桥正街183号 |
|
Applicant address: |
183 Xinqiao street, Shapingba District in Chongqing |
Study leader's address: |
183 Xinqiao street, Shapingba District in Chongqing |
|
申请注册联系人邮政编码: Applicant postcode: |
研究负责人邮政编码: Study leader's postcode: |
||
|
申请人所在单位: |
陆军军医大学新桥医院 |
||
|
Applicant's institution: |
Xinqiao Hospital Army Medical University |
||
|
研究负责人所在单位: |
陆军军医大学新桥医院 |
||
|
Affiliation of the Leader: |
Xinqiao Hospital Army Medical University |
||
|
是否获伦理委员会批准: |
是 |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
2022-研第442-02 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
|
批准本研究的伦理委员会名称: |
中国人民解放军陆军军医大学第二附属医院医学伦理会 |
||
|
Name of the ethic committee: |
Ethics Committee of The Second Affiliated Hospital of Army Medical University |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2022-12-16 00:00:00 | ||
|
伦理委员会联系人: |
刘丹 |
||
|
Contact Name of the ethic committee: |
Liu Dan |
||
|
伦理委员会联系地址: |
重庆市沙坪坝区新桥正街183号 |
||
|
Contact Address of the ethic committee: |
183 Xinqiao street, Shapingba District in Chongqing |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 23 6875 5422 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
KLL6324@163.com |
|
研究实施负责(组长)单位: |
陆军军医大学新桥医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Xinqiao Hospital Army Medical University |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
重庆市沙坪坝区新桥正街183号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
183 Xinqiao street, Shapingba District in Chongqing |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
无 |
||||||||||||||||||||||
|
Source(s) of funding: |
No |
||||||||||||||||||||||
|
研究疾病: |
T淋巴母细胞淋巴瘤和NK/T细胞淋巴瘤 |
||||||||||||||||||||||
|
Target disease: |
T lymphoblastic lymphoma and NK/T cell lymphoma |
||||||||||||||||||||||
|
研究疾病代码: |
|
||||||||||||||||||||||
|
Target disease code: |
|
||||||||||||||||||||||
|
研究类型: |
干预性研究 |
||||||||||||||||||||||
|
Study type: |
Interventional study |
||||||||||||||||||||||
|
研究所处阶段: |
探索性研究/预试验 | ||||||||||||||||||||||
|
Study phase: |
0 |
||||||||||||||||||||||
|
研究设计: |
单臂 |
||||||||||||||||||||||
|
Study design: |
Single arm |
||||||||||||||||||||||
|
研究目的: |
本研究是一项单臂、开放、多中心、探索性的临床研究,纳入NK/T细胞淋巴瘤、T淋巴母细胞淋巴瘤受试者,给予盐酸米托蒽醌脂质体注射液、依托泊苷,阿糖胞苷,环磷酰胺(PLMEAC),旨在探索PLMEAC联合方案的有效性和安全性。 |
||||||||||||||||||||||
|
Objectives of Study: |
To explore the effectiveness and safety of mitoxantrone hydrochloride liposome injection, etoposide, cytarabine and cyclophosphamide (PLMEAC) combined regimen in NK/T cell lymphoma and T lymphoblastic lymphoma. |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
|
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||
|
纳入标准: |
|||||||||||||||||||||||
|
Inclusion criteria |
|||||||||||||||||||||||
|
排除标准: |
1.心功能出现任意一种情况:(1)心脏功能受损或具有显著的心脏疾病:筛选前6个月内出现心肌梗塞,充血性心力衰竭,有症状需要药物治疗的心脏病,如不稳定性心绞痛、心律失常,未控制的重度高血压,6个月内发生过病毒性心肌炎或持续存在的心肌病病史;(2)心功能III级~IV级;(3)超声心动图左心室射血分数<60%;(4)在未安装心脏起搏器的情况下,12导联心电图出现II度/III度房室传导阻滞、长QT综合征或QTc>480 ms; 2.传染病筛查:乙型肝炎表面抗原阳性且HBV-DNA滴度超过研究中心上限,丙型病毒性肝炎抗体阳性且HCV-RNA滴度超过研究中心上限,人免疫缺陷病毒(HIV)抗体初筛阳性; 3.对任一PLMEAC药物成分有禁忌症; 4.伴有中枢神经系统淋巴瘤转移或软脑膜转移; 5.既往或当前合并有其他恶性肿瘤,除外经充分治疗的皮肤基底细胞癌或鳞状细胞癌、宫颈原位癌; 6.筛选前4周内患有急性症状性胰腺炎或慢性胰腺炎; 7.筛选前4周内进行过外科大手术或预计在研究期间进行大手术; 8.筛选前4周内患过严重感染,研究者判断不适合化疗; 9.有深静脉血栓或肺栓塞病史; 10.筛选时控制不佳的糖尿病; 11.筛选前3个月内活动性出血病史; 12.有药物(非医疗目的使用麻醉药品或精神药品)滥用史或药物(镇静催眠药、镇痛药、麻醉药、兴奋药及拟精神病性药物等)依赖史者; 13.任何精神疾病病史或认知障碍病史; 14.娠或哺乳期妇女或无论男女在12个月内有生育计划者; 15.研究者认为不适合参加本研究的其他情况。 |
||||||||||||||||||||||
|
Exclusion criteria: |
1.cardiac function: (1) impaired cardiac function or obvious heart disease: myocardial infarction, congestive heart failure, heart disease with symptoms requiring drug treatment, such as unstable angina pectoris, arrhythmia, uncontrolled severe hypertension, viral myocarditis or persistent cardiomyopathy within 6 months; (2).The cardiac function is Grade III ~IV; (3) Left ventricular ejection fraction < 60% by echocardiography; (4) In the absence of pacemaker, the 12-lead ECG showed II /III atrioventricular block, long QT syndrome or QTc>480 ms;; 2.Infectious disease screening: hepatitis B surface antigen is positive and HBV-DNA titer exceeds the upper limit of the research center, hepatitis C antibody is positive and HCV-RNA titer exceeds the upper limit of the research center, and human immunodeficiency virus (HIV) antibody is positive in the initial screening; 3.There are contraindications to any PLMEAC pharmaceutical ingredient; 4.Accompanied by central nervous system lymphoma metastasis or pia mater metastasis; 5.Other malignant tumors in the past or at present, except fully treated skin basal cell carcinoma or squamous cell carcinoma and cervical carcinoma in situ; 6.Suffering from acute symptomatic pancreatitis or chronic pancreatitis within 4 weeks before screening; 7.Major surgery has been performed within 4 weeks before screening or major surgery is expected; 8.Suffered from severe infection within 4 weeks before screening, and the researcher judged that chemotherapy was not suitable; 9. Have a history of deep vein thrombosis or pulmonary embolism; 10. Diabetes with poor control during screening; 11.History of active bleeding within 3 months before screening; 12.Those who have a history of drug abuse (using narcotic drugs or psychotropic drugs for non-medical purposes) or drug dependence (sedative hypnotics, analgesics, anesthetics, stimulants and quasi-psychotic drugs, etc.); 13.Any history of mental illness or cognitive impairment; 14.Pregnant or lactating women or those who have family planning within 12 months; 15.the researcher considers unsuitable to participate in this study. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2023-07-01 00:00:00至 To 2025-07-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-07-01 00:00:00 至 To 2025-07-01 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
|
||||||
|
性别: |
男女均可 |
Gender: |
Both |
||||||
|
随机方法(请说明由何人用什么方法产生随机序列): |
无 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
No |
||||||||
|
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 |
|
盲法: |
|
|
Blinding: |
|
|
试验完成后的统计结果(上传文件): |
|
|
Calculated Results after
|
|
|
是否共享原始数据: IPD sharing |
是Yes |
|
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): |
原始数据于试验结束后6个月以内采用临床试验公共管理平台向公众开放查询 |
|
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 |
|
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: |
原始数据采用临床试验公共平台进行记录和管理 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
The raw data will record and manage by the public management platform of clinical trials |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |