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注册号: Registration number: |
ChiCTR2500108454 |
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最近更新日期: Date of Last Refreshed on: |
2025-09-01 08:46:28 |
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注册时间: Date of Registration: |
2025-09-01 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: |
县级医院急性缺血性卒中血管再通治疗院内流程的调查研究 |
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Public title: |
Investigation on the workflow of intrahospital reperfusion therapy for acute ischemic stroke in county-level hospitals |
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注册题目简写: |
WIRIS研究 |
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English Acronym: |
WIRIS Trial |
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研究课题的正式科学名称: |
二级医院急性缺血性卒中院内再通治疗流程优化的建立与实践 |
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Scientific title: |
Establishment and practice of an optimized intrahospital reperfusion therapy for acute ischemic stroke in secondary hospitals |
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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: |
张振昶 |
研究负责人: |
张振昶 |
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Applicant: |
Zhang Zhenchang |
Study leader: |
Zhang Zhenchang |
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申请注册联系人电话: Applicant telephone: |
+86 138 9364 7595 |
研究负责人电话:
Study leader's |
+86 138 9364 7595 |
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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: |
13893647595@163.com |
研究负责人电子邮件: Study leader's E-mail: |
13893647595@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: |
甘肃省兰州市城关区萃英门82号 |
研究负责人通讯地址: |
甘肃省兰州市城关区萃英门82号 |
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Applicant address: |
82 Cuiyingmen, Chengguan District, Lanzhou City, Gansu Province, China |
Study leader's address: |
82 Cuiyingmen, Chengguan District, Lanzhou City, Gansu Province, 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: |
兰州大学第二医院(第二临床医学院) |
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Applicant's institution: |
The Second Hospital & Clinical Medical School, Lanzhou University |
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研究负责人所在单位: |
兰州大学第二医院(第二临床医学院) |
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Affiliation of the Leader: |
The Second Hospital & Clinical Medical School, Lanzhou 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: |
2025A-683 |
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: |
兰州大学第二医院(第二临床医学院)医学伦理委员会 |
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Name of the ethic committee: |
The Second Affiliated Hospital of the Second Hospital & Clinical Medical School, Lanzhou University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-07-03 00:00:00 | ||
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伦理委员会联系人: |
郑亚君 |
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Contact Name of the ethic committee: |
Zheng Yajun |
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伦理委员会联系地址: |
甘肃省兰州市城关区萃英门82号 |
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Contact Address of the ethic committee: |
82 Cuiyingmen, Chengguan District, Lanzhou City, Gansu Province, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 136 5932 6689 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
13659326689@163.com |
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研究实施负责(组长)单位: |
兰州大学第二医院(第二临床医学院) |
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Primary sponsor: |
The Second Hospital & Clinical Medical School, Lanzhou University |
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研究实施负责(组长)单位地址: |
甘肃省兰州市城关区萃英门82号 |
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Primary sponsor's address: |
82 Cuiyingmen, Chengguan District, Lanzhou City, Gansu Province, 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: |
癌症、心脑血管、呼吸和代谢性疾病防治研究国家科技重大专项 |
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Source(s) of funding: |
Noncommunicable Chronic Diseases-National Science and Technology Major Project |
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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: |
观察性研究 |
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Study type: |
Observational study |
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研究所处阶段: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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研究设计: |
横断面 |
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Study design: |
Cross-sectional |
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研究目的: |
分析以甘肃省为主的县级医院AIS院内再通治疗延误的影响因素,为优化县级医院AIS院内再通治疗流程提供真实依据。 |
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Objectives of Study: |
The aim is to analyze the factors affecting the delay of acute ischemic stroke (AIS) intrahospital reperfusion therapy in county-level hospitals (mainly in Gansu Province), and provide a real basis for optimizing the process of AIS intrahospital reperfusion therapy in county-level hospitals. |
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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. 经头颅CT或MRI证实颅内出血(包括脑实质出血、脑室内出血、蛛网膜下腔出血、硬膜下/外血肿等); 2. 既往颅内出血史; 3. 近3个月内有严重头外伤或卒中史; 4. 颅内肿瘤、巨大颅内动脉瘤; 5. 近期(3个月)有颅内或椎管内手术; 6. 近2周内大型外科手术; 7. 近3周内有胃肠或泌尿系统出血; 8. 活动性内脏出血; 9. 主动脉弓夹层; 10. 近1周内有在不易压迫止血部位的动脉穿刺; 11. 血压升高:收缩压>180 mmHg或舒张压>100 mmHg,并药物难以控制; 12. 急性出血倾向,包括血小板计数<100×109或其他情况; 13. 24h内接受过低分子肝素治疗; 14. 口服抗凝剂(华法林)且INR>1.7或PT>15 s; 15. 48 h内使用凝血酶抑制剂或Xa因子抑制剂,或各种实验室检查异常(如 APTT、INR、血小板计数、ECT、TT或Xa因子活性测定等); 16. 血糖<2.8或>22.22 mmol/L,并难以纠正; 17. 头颅CT或MRI提示大面积梗死(梗死面积>1/3大脑中动脉供血区); 18. 孕产妇; 19. 院内卒中; 20. 诊断检查不确定或显示卒中以外的可能原因的事件。 |
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Exclusion criteria: |
1. Intracranial hemorrhage confirmed by cranial computed tomography (CT) or magnetic resonance imaging (MRI), including cerebral parenchymal hemorrhage, intraventricular hemorrhage, subarachnoid hemorrhage, subdural/extradural hematoma, etc; 2. History of prior intracranial hemorrhage; 3. Severe head trauma or stroke within the past 3 months; 4. Intracranial tumor, giant intracranial aneurysm; 5. Intracranial or intraspinal surgery within 3 months; 6. Major surgical procedures within the past 2 weeks; 7. Gastrointestinal or genitourinary bleeding within the past 3 weeks; 8. Active visceral bleeding; 9. Aortic arch dissection; 10. Arterial puncture at a non-compressible site within the previous week; 11. Elevated blood pressure: systolic pressure >180 mmHg or diastolic pressure >100 mmHg, and difficult to control with medication; 12. Acute bleeding tendency, including platelet count <100×10⁹/L or other conditions; 13. Treatment with low molecular weight heparin within 24 hours; 14. Use of oral anticoagulants (e.g., warfarin) with INR >1.7 or PT >15 s; 15. Use of thrombin inhibitors or Xa factor inhibitors within 48 hours, or abnormal laboratory tests (such as APTT, INR, platelet count, ECT, TT, or Xa factor activity assay, etc.); 16. Blood glucose level <2.8 mmol/L or >22.22 mmol/L, and difficult to correct; 17.Head CT or MRI indicates a large area of infarction (infarction area>1/3 of the middle cerebral artery supply area); 18. Pregnancy or postpartum status; 19. In-hospital stroke; 20. Diagnostic workup is uncertain or suggests an event other than stroke as the likely cause. |
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研究实施时间: Study execute time: |
从 From 2025-09-01 00:00:00至 To 2026-08-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-09-01 00:00:00 至 To 2026-08-31 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): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
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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: |
无 |
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Blinding: |
None |
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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). |
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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). |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |