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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: |
ChiCTR2000029117 |
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最近更新日期: Date of Last Refreshed on: |
2020-02-11 18:10:37 |
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注册时间: Date of Registration: |
2020-01-14 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: |
注射用益气复脉(冻干)治疗急性心力衰竭疗效的多中心双盲随机对照试验 |
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Public title: |
Auxiliary Strategy of Yiqi Fumai Lyophilized Injection on Standard Therapy in Acute Heart Failure |
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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: |
冠心病 (心绞痛-心肌梗死-心衰) 中医药防治方案的循证优化及疗效机制 |
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Scientific title: |
Evidence-Based Optimization and Therapeutic Mechanism of Traditional Chinese Medicine in Prevention and Treatment of Coronary Heart Disease (Angina Pectoris-Myocardial Infarction-Heart Failure) |
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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: |
ChiMCTR2000002994 |
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申请注册联系人: |
张晶晶 |
研究负责人: |
商洪才 |
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Applicant: |
Zhang Jingjing |
Study leader: |
Shang Hongcai |
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申请注册联系人电话: Applicant telephone: |
+86 18810212201 |
研究负责人电话: Study leader's telephone: |
+86 18202525733 |
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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: |
zjhzyyfy@163.com |
研究负责人电子邮件: Study leader's E-mail: |
shanghongcai@126.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: |
北京市朝阳区北三环东路11号 |
研究负责人通讯地址: |
北京市东城区海运仓胡同5号 |
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Applicant address: |
11 North Third Ring Road East, Chaoyang District, Beijing |
Study leader's address: |
5 Haigangcang Lane, 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 |
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Applicant's institution: |
Beijing University of 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 Affiliated to Beijing University of Chinese Medicine |
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是否获伦理委员会批准: |
是/Yes |
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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: |
DZMEC-KY-2019-166 |
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: |
Ethics Committee of Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine |
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伦理委员会批准日期: Date of approved by ethic committee: |
2019-11-14 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: |
北京中医药大学东直门医院 |
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Primary sponsor: |
Dongzhimen Hospital Affiliated to Beijing University of 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胡同5号 |
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Primary sponsor's address: |
5 Haigangcang Lane, 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: |
本课题来源于2017年国家重点研发计划“中医药现代化研究”重点专项 ——冠心病心衰中医综合治疗方案循证优化研究(2017YFC1700403),经费来源于国家科技部 |
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Source(s) of funding: |
This work was financially supported by the National Key Research and Development Plan (2017YFC1700400, 2017YFC1700403) |
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Target disease: |
Acute Heart Failure |
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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: |
在急性心力衰竭常规治疗的基础上加载益气复脉(冻干)注射剂,采用多中心、双盲、随机、安慰剂平行对照设计方法,观察患者90天全因死亡或因心衰再入院率,评价注射用益气复脉(冻干)治疗急性心力衰竭的有效性和安全性。 |
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Objectives of Study: |
On the basis of routine treatment of acute heart failure, Yiqi Fumai (freeze-dried) injection was added, and a multicenter, double-blind, randomized, placebo parallel control design was used to observe the rate of death or readmission due to heart failure for 90 days. To evaluate the efficacy and safety of Yiqi Fumai (lyophilized) for injection in the treatment of acute heart failure. |
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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. 明确诊断急性心力衰竭入院患者; |
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Inclusion criteria |
1. Clearly diagnose patients admitted to acute heart failure; |
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排除标准: |
1. 筛选期收缩压持续性≤90mmHg; |
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Exclusion criteria: |
1. The duration of systolic blood pressure during the screening period was less than 90mmHg. |
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研究实施时间: Study execute time: |
从 From 2019-10-01 00:00:00至 To 2021-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2020-02-01 00:00:00 至 To 2021-09-30 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: |
尚未开始 Not yet 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): |
采用第三方中央随机化系统,试验组和对照组的比例为 1:1。受试者筛选成功后,由分中心研究者登录中央随机化系统,根据系统提示输入受试者基本信息,随机系统给出受试者编码和随机号,每位受试者的编码和随机号均是唯一且被相互绑定的。随机号产生后,由药物管理员再次登录IWRS,根据分组提示信息,告知研究护士受试者组别,并发放药物给研究护士配置使用. |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
The third-party central randomization system (IWRS), The ratio between the test group and the control group was 1:1. |
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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: |
双盲 |
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Blinding: |
Double blind |
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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 |
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): |
公开数据的时间为试验完成后的6个月内,方式为:联系统计师 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
The time to disclose the data is within 6 months of the completion of the trial by: Contacting the statistician |
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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: |
病例报告表(CRF)由纸质版与电子数据库录入两种方式组成,纸质版 CRF为无碳复写、一式二份,由研究者填写,电子CRF在纸质版填写后需及时录入。每个受试者的数据必须完成两种CRF的填写。监查员(CRA) 应定期现场监查CRF,保证纸质CRF与电子CRF一致性,发现的问题与研究者核实后由研究者修改签字。完成后的纸质版CRF由CRA和各分中心的主要研究者审核签字后,向数据管理单位提交第一联。CRF提交后,由数据管理团队进行逻辑数据审核。如对数据有疑问,由数据管理员发出“电子数据质询”至CRA及研究者,并通过CRA向研究者发出询问,研究者应尽快解答并返回,数据管理员根据研究者的回答进行数据修改、确认。所有错误内容及修改结果应有记录并妥善保存。纸质CRF在研究者、CRA、数据管理员之间的传递应有专门的记录并妥善保存。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
The case report form (CRF) is composed of paper version and electronic database. The paper version CRF is carbon-free and duplicates, which is filled out by researchers. Electronic CRF should be entered in time after the paper version is filled out. The data for each subject must be filled in in two types of CRF. The inspector (CRA) shall regularly monitor the CRF, on the spot to ensure that the paper CRF is consistent with the electronic CRF, and the problems found shall be verified with the researcher and modified and signed by the researcher. The completed paper version of CRF is reviewed and signed by CRA and the main researchers of each sub-center, and the first joint is submitted to the data management unit. After the CRF is submitted, the logical data review is carried out by the data management team. If there is any doubt about the data, the data administrator will issue an "electronic data challenge" to CRA and the researcher, and send the inquiry to the researcher through CRA. The researcher should answer the question and return it as soon as possible. The data administrator modifies and confirms the data according to the researcher's answer. All errors and modification results should be recorded and properly preserved. The transfer of paper CRF between researchers, CRA and data administrators should be specially recorded and properly preserved. |
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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 |