|
审核状态: Project audit state: |
通过审核 Successful |
|
注册号: Registration number: |
ChiCTR2600122697 |
|
最近更新日期: Date of Last Refreshed on: |
2026-04-16 15:49:41 |
|
注册时间: Date of Registration: |
2026-04-16 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
骨髓增殖性肿瘤患者的治疗模式与患者体验调查 |
|
Public title: |
Survey on treatment patterns and patient experience among myeloproliferative neoplasm patients |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
骨髓增殖性肿瘤患者的治疗模式与患者体验调查 |
|
Scientific title: |
Survey on treatment patterns and patient experience among myeloproliferative neoplasm patients |
|
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: |
张静 |
研究负责人: |
张磊 |
|
Applicant: |
Zhang Jing |
Study leader: |
Zhang Lei |
|
申请注册联系人电话: Applicant telephone: |
+86 186 4111 7998 |
研究负责人电话:
Study leader's |
+86 22 2390 9095 |
|
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: |
zhangjing2556@163.com |
研究负责人电子邮件: Study leader's E-mail: |
ec@ihcams.ac.cn |
|
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: |
上海市徐汇区吴中路8号锦辉大厦818室 |
研究负责人通讯地址: |
天津市和平区南京路288号 |
|
Applicant address: |
Room 818, Jinhui Building, No. 8 Wuzhong Road, Xuhui District, Shanghai |
Study leader's address: |
No. 288, Nanjing Road, Heping District, Tianjin, China? |
|
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: |
上海信华医药科技有限公司 |
||
|
Applicant's institution: |
Shanghai Xincere Med Tech Inc. |
||
|
研究负责人所在单位: |
中国医学科学院血液病医院(中国医学科学院血液学研究所) |
||
|
Affiliation of the Leader: |
Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences |
||
|
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: |
QT2026001-EC-1 |
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: |
中国医学科学院血液病医院(中国医学科学院血液学研究所)伦理审查委员会 |
||
|
Name of the ethic committee: |
Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences EC Committee |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2026-03-05 00:00:00 | ||
|
伦理委员会联系人: |
王老师 |
||
|
Contact Name of the ethic committee: |
+86 022-23909095 |
||
|
伦理委员会联系地址: |
天津市静海区团泊大道28号 |
||
|
Contact Address of the ethic committee: |
NO.28 Tuanbo Road, Jinghai District, Tianjin |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 22 2360 8025 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
|
|
研究实施负责(组长)单位: |
中国医学科学院血液病医院(中国医学科学院血液学研究所) |
||||||||||||||||||||||
|
Primary sponsor: |
Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
天津市和平区南京路288号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
No. 288, Nanjing Road, Heping District, Tianjin, China? |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
默沙东(中国)投资有限公司 |
||||||||||||||||||||||
|
Source(s) of funding: |
MSD (CHINA) HOLDING CO.,LTD |
||||||||||||||||||||||
|
研究疾病: |
骨髓增殖性肿瘤(原发性血小板增多症、真性红细胞增多症) |
||||||||||||||||||||||
|
Target disease: |
Myeloproliferative Neoplasms (Essential Thrombocythemia, Polycythemia Vera) |
||||||||||||||||||||||
|
研究疾病代码: |
|
||||||||||||||||||||||
|
Target disease code: |
|
||||||||||||||||||||||
|
研究类型: |
观察性研究 |
||||||||||||||||||||||
|
Study type: |
Observational study |
||||||||||||||||||||||
|
研究所处阶段: |
其它 | ||||||||||||||||||||||
|
Study phase: |
N/A |
||||||||||||||||||||||
|
研究设计: |
横断面 |
||||||||||||||||||||||
|
Study design: |
Cross-sectional |
||||||||||||||||||||||
|
研究目的: |
描述MPN患者的特征和治疗模式;描述MPN患者的临床诊断和治疗历程;识别影响治疗选择的决策因素;评估疾病负担及其对生活质量的影响;探索未满足的临床需求。 |
||||||||||||||||||||||
|
Objectives of Study: |
1.To describe the characteristics and treatment patterns of ET/PV patients. 2.To describe the clinical diagnosis and treatment journeys of ET/PV patients. 3.To identify the decision-making factors influencing treatment choices. 4.To assess disease burden and its impact on quality of life. 5.To explore clincal unmet needs. |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
|
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||
|
纳入标准: |
血液科医生入选标准: 1. 过去12个月内具有MPN患者管理经验,定义为:“在过去12个月内至少诊断并治疗过8例MPN患者,其中需包含至少2例PV患者和4例ET患者”。 2. 所有参与者必须签署知情同意书或阅读《参与者须知函》。 患者入选标准: 1. 年龄≥18岁; 2. 经门诊确诊为PV或ET; 3.已接受过治疗的患者 ; 4. 所有受试者必须签署知情同意书或阅读《参与者须知函》。 |
||||||||||||||||||||||
|
Inclusion criteria |
Hematology Physicians: 1. Having experience in managing MPN patients within the past 12 months, defined as having diagnosed and treated at least 8 MPN patients in the past 12 months, including at least 2 patients with PV and at least 4 patients with ET. 2. All participants must provide informed consent or read through the Participant Info Letter. Patients: 1. Aged ≥18 years ; 2. Diagnosed with PV or ET by clinic visit; 3. Patients who have received treatment; 4. All subjects must provide informed consent or read through the Participant Info Letter. |
||||||||||||||||||||||
|
排除标准: |
患者目前正在接受默克/MSD疗法或同类药物治疗。 |
||||||||||||||||||||||
|
Exclusion criteria: |
Patients are currently receiving Merck/MSD therapy or therapy with drugs in the same class. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2026-03-31 00:00:00至 To 2027-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-04-29 00:00:00 至 To 2026-11-30 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): |
None |
||||||||
|
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 |
否No |
|
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): |
无 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
NA |
|
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: |
数据采集采用结构化问卷调查,医生问卷通过在线平台完成,患者问卷由研究者线下面对面收集后人工录入系统。数据管理采用信华自主研发的电子数据采集和管理系统,统计分析使用SAS软件(9.3或以上版本)。所有数据在分析前进行去标识化处理,严格遵循保密原则。 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Data were collected using structured questionnaires. Physician questionnaires were completed via an online platform, while patient questionnaires were collected face-to-face by investigators and manually entered into the system by patient themselves . Data management was performed using Xincere's self-developed electronic data capture and management system, and statistical analyses were conducted using SAS software (version 9.3 or higher). All data were de-identified prior to analysis, and strict confidentiality principles were followed. |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |