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注册号: Registration number: |
ChiCTR-INR-17014167 |
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最近更新日期: Date of Last Refreshed on: |
2021-09-07 02:16:21 |
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注册时间: Date of Registration: |
2017-12-27 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
替罗非班联合血管再通治疗急性缺血性卒中 |
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Public title: |
Revascularization pretreated with tirofiban for acute ischemic stroke |
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注册题目简写: |
RESCUE BT |
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English Acronym: |
RESCUE BT |
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研究课题的正式科学名称: |
发病24小时内急性前循环大血管闭塞性卒中比较替罗非班联合血管内治疗与单独血管内治疗安全性及有效性的多中心、前瞻性、随机、双盲、安慰剂对照临床试验 |
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Scientific title: |
Tirofiban plus endovascular treatment versus endovascular treatment alone for acute anterior large vessel occlusive stroke within 24 hours of symptom onset: a multi-center, prospective, randomized, double-blind, placebo-controlled clinical 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: |
邱忠明 |
研究负责人: |
杨清武 |
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Applicant: |
Zhongming Qiu |
Study leader: |
Qingwu Yang |
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申请注册联系人电话: Applicant telephone: |
+86 13236599269 |
研究负责人电话:
Study leader's |
+86 13657638868 |
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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: |
qiuzhongmingdoctor@163.com |
研究负责人电子邮件: Study leader's E-mail: |
yangqwmlys@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: |
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 |
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Applicant address: |
183 Xinqiao Main Street, Shapingba District, Chongqing, China |
Study leader's address: |
183 Xinqiao Main Street, Shapingba District, Chongqing, 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: |
第三军医大学新桥医院 |
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Applicant's institution: |
Xinqiao Hospital, the Third Military Medical University |
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研究负责人所在单位: |
第三军医大学新桥医院 |
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Affiliation of the Leader: |
Xinqiao Hospital, the Third Military 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: |
ChiECRCT-20180012 |
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: |
中国注册临床试验伦理审查委员会 |
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Name of the ethic committee: |
Chinese Ethics Committee of Registering Clinical Trials |
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伦理委员会批准日期: Date of approved by ethic committee: |
2018-02-08 00:00:00 | ||
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伦理委员会联系人: |
米娜 |
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Contact Name of the ethic committee: |
Mina |
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伦理委员会联系地址: |
中国香港特别行政区九龙塘浸会大学中国临床试验注册中心香港中心 |
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Contact Address of the ethic committee: |
Chinese Clinical Trial Registry Hong Kong Center, Hong Kong Baptist University, Hong Kong SAR, 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: |
第三军医大学新桥医院 |
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Primary sponsor: |
Xinqiao Hospital, the Third Military 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183号 |
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Primary sponsor's address: |
183 Xinqiao Main Street, Shapingba District, Chongqing, 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: |
经费自筹 |
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Source(s) of funding: |
self-financing |
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研究疾病: |
急性缺血性卒中 |
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Target disease: |
acute ischemic stroke |
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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: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
探讨血管内治疗前经静脉给予替罗非班抗血小板治疗在发病24小时前循环大动脉闭塞性卒中患者中的有效性及安全性。 |
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Objectives of Study: |
To investigate the effectiveness and safety of endovascular treatment pretreated with tirofiban in acute ischemic stroke patients due to large artery occlusion in the anterior circulation within 24 hours of stroke onset. |
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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: |
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Inclusion criteria |
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排除标准: |
(1) CT或MR证实为脑出血; |
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Exclusion criteria: |
(1) CT or MR evidence of hemorrhage; |
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研究实施时间: Study execute time: |
从 From 2017-12-01 00:00:00至 To 2022-03-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2018-11-10 00:00:00 至 To 2021-11-30 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): |
患者按照1:1比例被随机分成两组。本试验采用分层区组随机化的方法进行随机化分组,按照各分中心以1:1比例产生随机分组序列。各分中心研究者在患者签署知情同意书后,通过“金陵鼠”APP(Random Allocation Tool,RAT 1.1)实现随机化分组。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Subjects will be randomly allocated to two groups in a 1:1 ratio. To produce a randomization sequence in a 1:1 ratio, stratified block randomization is used in this study according to subcentres. After obtaining written informed consent from patients and/or their relatives, investigators achieve randomization by& |
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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: |
未说明 |
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Blinding: |
Not stated |
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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 |
是Yes |
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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): |
相关论文发表5年后在Resman平台公开原始数据 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Related papers published five years later, the IPD will be shared on ResMan. |
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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: |
采用病例报告表(CRF)和临床试验电子数据采集系统(EDC)ResMan采集与管理数据 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Use Case Record Form (CRF) and Electronic Data Capture (EDC), ResMan to collect and manage data. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |