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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: |
ChiCTR-ONC-13003844 |
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最近更新日期: Date of Last Refreshed on: |
2015-05-02 20:38:15 |
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注册时间: Date of Registration: |
2013-11-04 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: |
在实际临床环境中进行计算机断层扫描血管造影(CTA)检查的受试者使用碘克沙醇270 mg I/mL的开放性、前瞻性、多中心、非干预研究 |
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Public title: |
An Open Label, Prospective, Multicentre, Non-interventional Study of Iodixanol 270 mg I/mL for Use in Subjects Undergoing Computed Tomographic Angiography (CTA) Examinations in Real World Clinical Practice |
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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: |
在实际临床环境中进行计算机断层扫描血管造影(CTA)检查的受试者使用碘克沙醇270 mg I/mL的开放性、前瞻性、多中心、非干预研究 |
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Scientific title: |
An Open Label, Prospective, Multicentre, Non-interventional Study of Iodixanol 270 mg I/mL for Use in Subjects Undergoing Computed Tomographic Angiography (CTA) Examinations in Real World Clinical Practice |
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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: |
李坤成 |
研究负责人: |
李坤成 |
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Applicant: |
Li kuncheng |
Study leader: |
Li kuncheng |
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申请注册联系人电话: Applicant telephone: |
+86 13911099059 |
研究负责人电话:
Study leader's |
+86 13911099059 |
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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: |
cjr.likuncheng@vip.163.com |
研究负责人电子邮件: Study leader's E-mail: |
cjr.likuncheng@vip.163.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: |
北京市西城区长椿街45号 |
研究负责人通讯地址: |
北京市西城区长椿街45号 |
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Applicant address: |
No.45 Changchun Street, Xicheng District, Beijing |
Study leader's address: |
No.45 Changchun Street, Xicheng District, Beijing |
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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: |
首都医科大学宣武医院 |
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Applicant's institution: |
Xuanwu Hospital of Capital Medical University |
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研究负责人所在单位: |
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Affiliation of the Leader: |
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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: |
临药审【2013】018号 |
伦理委员会批件附件: Approved file of Ethical Committee: |
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批准本研究的伦理委员会名称: |
首都医科大学宣武医院伦理委员会 |
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Name of the ethic committee: |
Xuanwu Hospital of Capital Medical University, Ethic Commitee |
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伦理委员会批准日期: Date of approved by ethic committee: |
2013-09-23 00:00:00 | ||
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伦理委员会联系人: |
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Contact Name of the ethic committee: |
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伦理委员会联系地址: |
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Contact Address of the ethic committee: |
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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: |
首都医科大学宣武医院 |
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Primary sponsor: |
Xuanwu Hospital of Capital Medical University |
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研究实施负责(组长)单位地址: |
北京市西城区长椿街45号 |
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Primary sponsor's address: |
No.45 Changchun Street, Xicheng District, Beijing |
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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: |
通用电气药业(上海)有限公司 |
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Source(s) of funding: |
GE Healthcare (Shanghai) Co.Ltd |
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研究疾病: |
冠状动脉/主动脉、头颈动脉、肾动脉和肺动脉相关疾病 |
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Target disease: |
coronary, aortic, head and neck, renal and pulmonary arteries relative conditions |
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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: |
1.评价属于实际临床环境下常规医疗的一部分,对进行冠状动脉/主动脉、头颈动脉、肾动脉和肺动脉CTA的受试者给予碘克沙醇270mgI/mL后,采用100kVp扫描方案及迭代重建算法的对比增强和成像质量 2.评价目标受试者人群中碘克沙醇270 mg I/mL给药后的总体受试者安全性 |
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Objectives of Study: |
1.To evaluate the contrast enhancement and imaging quality following administration of iodixanol 270 mgI/mL with a 100kVp scanning protocol and iterative noise-reducing image reconstruction software in; 2.To evaluate the overall subject safety profile after administration of iodixanol 270 mg I/mL in the targeted subject population. |
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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) 年满18岁。 |
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Inclusion criteria |
(1) The subject is over 18 years old;(2) Subjects are referred to undergo CTA examination of coronary, aortic, head and neck, renal and pulmonary arteries as part of their routine clinical care; (3) The subject has provided a signed and dated informed consent. |
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排除标准: |
(1) 已知对含碘对比剂过敏,包括但不限于荨麻疹、过敏样反应或心血管反应、喉部水肿和支气管痉挛。 |
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Exclusion criteria: |
(1) Subject has a known allergy to iodinated contrast agent, including but not limited to hives, anaphylactoid or cardiovascular reactions, laryngeal oedema, and bronchospasm; |
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研究实施时间: Study execute time: |
从 From 2013-08-01 00:00:00至 To 2015-02-28 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2013-08-01 00:00:00 至 To 2015-02-28 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): |
非干预 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Non-interventional |
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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 |
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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): |
方恩(天津)医药发展有限公司公司 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Fountain Medical (TIANJIN) Co., Ltd |
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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: |
方恩(天津)医药发展有限公司公司 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Fountain Medical (TIANJIN) Co., Ltd |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |