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注册号: Registration number: |
ChiCTR2500110680 |
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最近更新日期: Date of Last Refreshed on: |
2025-10-17 15:59:34 |
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注册时间: Date of Registration: |
2025-10-17 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: |
脑心安胶囊治疗中风病观察性疗效比较研究 |
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Public title: |
Comparative study on observational efficacy of Naoxin'an capsule in the treatment of stroke |
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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: |
脑心安胶囊治疗中风病观察性疗效比较研究 |
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Scientific title: |
Comparative study on observational efficacy of Naoxin'an capsule in the treatment of stroke |
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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: |
陈媛媛 |
研究负责人: |
孔令博 |
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Applicant: |
Chen Yuanyuan |
Study leader: |
Kong Lingbo |
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申请注册联系人电话: Applicant telephone: |
+86 182 0894 6889 |
研究负责人电话:
Study leader's |
+86 131 6732 3987 |
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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: |
3043623634@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
klb1984@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: |
北京市东城区海运仓5号 |
研究负责人通讯地址: |
北京市东城区海运仓5号 |
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Applicant address: |
5 Haihaicang, Dongcheng District, Beijing |
Study leader's address: |
5 Haihaicang, Dongcheng 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: |
北京中医药大学东直门医院 |
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Applicant's institution: |
Dongzhimen Hospital of Beijing University of Traditional Chinese Medicine |
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研究负责人所在单位: |
北京中医药大学东直门医院 |
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Affiliation of the Leader: |
Dongzhimen Hospital of Beijing University of Traditional Chinese Medicine |
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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: |
2023DZMEC-007-01 |
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: |
北京中医药大学东直门医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Dongzhimen Hospital of Beijing University of Traditional Chinese Medicine |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-01-13 00:00:00 | ||
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伦理委员会联系人: |
韩雪婷 |
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Contact Name of the ethic committee: |
Han Xueting |
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伦理委员会联系地址: |
北京市东城区海运仓5号 |
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Contact Address of the ethic committee: |
5 Haihaicang, Dongcheng District, Beijing |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 10 8401 2709 |
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: |
北京中医药大学东直门医院 |
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Primary sponsor: |
Dongzhimen Hospital of Beijing University of Traditional Chinese Medicine |
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研究实施负责(组长)单位地址: |
北京市东城区海运仓5号 |
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Primary sponsor's address: |
5 Haihaicang, Dongcheng 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: |
吉林意达药业有限公司 |
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Source(s) of funding: |
Jilin Yida Pharmaceutical Co., Ltd |
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研究疾病: |
脑血管疾病 |
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Target disease: |
Cerebrovascular disease |
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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.探讨脑心安胶囊在临床中治疗中风病的临床实际应用特点和优势; 2.比较脑心安胶囊不同分期及用药疗程对中风患者预后影响的差异; 3.探讨脑心安胶囊对中风病合并冠心病患者的疗效作用; 4.探讨脑心安胶囊对心脑血管联合事件的防治作用; 5.开展脑心安胶囊治疗中风病的经济学评价; |
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Objectives of Study: |
1.To explore the characteristics and advantages of clinical application of Naoxin'an capsule in the treatment of stroke; 2.To compare the effects of different stages and treatment courses of Naoxin'an capsule on the prognosis of stroke patients; 3.To explore the therapeutic effect of Naoxin'an capsule on patients with stroke and coronary heart disease; 4.To explore the preventive and therapeutic effects of Naoxin'an capsule on combined cardiovascular and cerebrovascular events; 5.Carry out economic evaluation of Naoxin'an capsule in the treatment of stroke; |
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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.已知对脑心安胶囊或相关药物成份过敏者。 2.既往有卒中病史且遗留后遗症影响结局测评者,即本次卒中发病前mRS 得分≥2 分。 3.合并严重肝、肾功能不全者(备注:严重肝功能不全定义为ALT 或AST 大于3倍正常上限;严重肾功能不全定义为血肌酐值大于2 倍正常上限。 4.患有其他威胁生命的严重疾病,预期生存时间小于3 个月者。 5.妊娠、计划妊娠或哺乳期妇女。 6.合并显著限制神经功能评价或影响病人随访的其他疾病。 7.病人或其护理人员不能配合完成随访工作。 |
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Exclusion criteria: |
1. People who are known to be allergic to Naoxin'an capsules or related pharmaceutical ingredients; 2.Those who have a previous history of stroke and have residual sequelae that affect the outcome evaluation, i.e., the mRS score before the onset of this stroke is >= 2 points; 3.Patients with severe liver and renal insufficiency (Note: Severe liver insufficiency is defined as ALT or AST greater than 3 times the upper limit of normal; severe renal insufficiency is defined as blood creatinine greater than 2 times the upper limit of normal; 4.Patients with other life-threatening serious diseases with an expected survival time of less than 3 months; 5.Pregnant, planned, or lactating women; 6.Other diseases that significantly limit the evaluation of neurological function or affect patient follow-up; 7.Patients or their caregivers cannot cooperate in completing follow-up work. |
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研究实施时间: Study execute time: |
从 From 2022-07-01 00:00:00至 To 2027-06-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-09-01 00:00:00 至 To 2027-06-30 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): |
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: |
不公开/Private |
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盲法: |
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Blinding: |
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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): |
研究结束后6个月,临床试验公共管理平台http://www.medresman.org.cn/ |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Six months after the study ends, Clinical Trial Public Management Platform http://www.medresman.org.cn/ |
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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: |
一般情况下,研究对象病史和临床用药信息以住院病历为源数据;实验室检查和功能检查结果以HIS或检验科信息系统为源数据。量表数据可以直接记录在eCRF的数据或研究者另外提供的可识别对象和时间的书面记录为源数据。研究者及供职的医疗机构应允许申办方的监查员、稽查员、伦理委员会的审查者直接查阅临床研究相关的源数据和源文件。本研究采用电子病历采集系统,http://1-dao.net:13579/Login/ClinicIndex,所有数据由平台管理人员负责数据的收集、整理及保管,在系统中设计逻辑核查条件以协助控制数据缺失和逻辑错误。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
In general, the medical history and clinical medication information of the research subjects are sourced from inpatient medical records; Laboratory and functional test results are sourced from HIS or laboratory information systems. Scale data can be directly recorded in eCRF data or written records of identifiable objects and times provided by researchers as source data. Researchers and medical institutions should allow the sponsor's supervisors, auditors, and ethics committee reviewers to directly access source data and files related to clinical research. This study utilizes an electronic medical record collection system (accessible at http://1-dao.net:13579/Login/ClinicIndex). All data are collected, organized, and maintained by the platform administrators. Logic check conditions have been implemented within the system to assist in controlling data omissions and logical errors. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |