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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: |
ChiCTR2100048734 |
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最近更新日期: Date of Last Refreshed on: |
2021-07-15 00:48:49 |
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注册时间: Date of Registration: |
2021-07-15 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: |
洛珊治疗中国精神分裂症患者的安全性和有效性的上市后重点监测 |
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Public title: |
Safety and Effectiveness of Lonasen Post-marketing Surveillance in Treatment of Chinese Schizophrenia Patients |
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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: |
布南色林治疗中国精神分裂症患者的安全性和有效性的上市后重点监测 |
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Scientific title: |
Safety and Effectiveness of Blonanserin Post-marketing Surveillance in Treatment of Chinese Schizophrenia Patients |
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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: |
李海云 |
研究负责人: |
陈晋东 |
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Applicant: |
Li Haiyun |
Study leader: |
Chen Jindong |
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申请注册联系人电话: Applicant telephone: |
+86 13601803116 |
研究负责人电话:
Study leader's |
+86 0731-85295888 |
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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: |
lihaiyun@dsmpharm.com.cn |
研究负责人电子邮件: Study leader's E-mail: |
chenjindong@csu.edu.cn |
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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: |
上海市黄陂南路838弄 |
研究负责人通讯地址: |
长沙市人民中路139号 |
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Applicant address: |
838th Lane, South Huangpi Road, Shanghai, China |
Study leader's address: |
139 Renmin Middle Road, Changsha, Hu'nan, China |
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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: |
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申请人所在单位: |
住友制药(苏州)有限公司 |
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Applicant's institution: |
Sumitomo Pharmaceuticals (Suzhou) Co., Ltd. |
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研究负责人所在单位: |
中南大学湘雅二医院 |
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Affiliation of the Leader: |
The Second Xiangya Hospital of Central South 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: |
(2018)伦审【科】第【093】号 |
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: |
中南大学湘雅二医院医学伦理委员会 |
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Name of the ethic committee: |
Ethics committee of the Second Xiangya Hospital of Central South University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2018-11-28 00:00:00 | ||
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伦理委员会联系人: |
舒畅 |
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Contact Name of the ethic committee: |
Shu Chang |
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伦理委员会联系地址: |
长沙市人民中路139号 |
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Contact Address of the ethic committee: |
139 Renmin Middle Road, Changsha, Hu'nan, 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: |
中南大学湘雅二医院 |
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Primary sponsor: |
The Second Xiangya Hospital of Central South University |
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研究实施负责(组长)单位地址: |
中国-湖南-长沙市人民中路139号 |
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Primary sponsor's address: |
139 Renmin Middle Road, Changsha, Hu'nan, 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: |
住友制药(苏州)有限公司 |
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Source(s) of funding: |
Sumitomo Pharmaceutical (Suzhou) Co., Ltd. |
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研究疾病: |
精神分裂症 |
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Target disease: |
Schizophrenia |
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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: |
连续入组 |
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Study design: |
Sequential |
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研究目的: |
了解布南色林用于真实世界中的中国精神分裂症患者的安全性以及布南色林单药或与其他药物合并使用的总体疗效情况以及剂量情况。 |
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Objectives of Study: |
To investigate the safety profile of blonanserin for Chinese patients with schizophrenia in the real world and the overall effectiveness and dosage of blonanserin monotherapy or combination therapy. |
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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: |
开始使用布南色林的精神分裂症患者 |
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Inclusion criteria |
Schizophrenia Patients who begin to receive blonanserin |
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排除标准: |
无 |
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Exclusion criteria: |
No exclusion criteria |
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研究实施时间: Study execute time: |
从 From 2018-09-01 00:00:00至 To 2022-01-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2018-09-01 00:00:00 至 To 2021-10-31 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): |
不适用 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
NA |
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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): |
项目组根据国家药品监督管理局药品评价中心要求、研究进程择期选择具体方式公开原始数据 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
The original data will be disclosed according to the requirements of the National center for ADR monitoring and the research process |
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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: |
本研究采用电子化数据管理,使用DAS for EDC (V5.0) 数据管理员根据试验方案设计eCRF,数据库构建人员Database Designer构建数据库,并根据逻辑核查计划(DVP)设置逻辑核查,通过测试并获申办方批准后发布使用 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
This study uses electronic data management [DAS for EDC (V5.0)]. The Data Manager designs the eCRF based on the study protocol, Database Designer set up the database and logic verification according to the logical verification plan (DVP) which could release to use after passing the test and approved by the sponsor. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |