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注册号: Registration number: |
ChiCTR2300079180 |
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最近更新日期: Date of Last Refreshed on: |
2023-12-27 09:08:19 |
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注册时间: Date of Registration: |
2023-12-27 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: |
乌司他丁对低血容量性休克患者早期复苏影响的前瞻性、多中心、队列研究 |
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Public title: |
The Effect of Ulinastatin on Early Resuscitation in Patients with Hypovolemic Shock:A Prospective, Multicenter, Cohort Study |
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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: |
乌司他丁对低血容量性休克患者早期复苏影响的前瞻性、多中心、队列研究 |
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Scientific title: |
The Effect of Ulinastatin on Early Resuscitation in Patients with Hypovolemic Shock:A Prospective, Multicenter, Cohort Study |
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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: |
黎奕宏 |
研究负责人: |
蒋龙元 |
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Applicant: |
Li Yihong |
Study leader: |
Jiang Longyuan |
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申请注册联系人电话: Applicant telephone: |
+86 166 2047 0210 |
研究负责人电话:
Study leader's |
+86 133 1280 9001 |
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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: |
lyh122580210@163.com |
研究负责人电子邮件: Study leader's E-mail: |
jly1964@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: |
广东省广州市越秀区沿江西路107号中山大学孙逸仙纪念医院 |
研究负责人通讯地址: |
广东省广州市越秀区沿江西路107号中山大学孙逸仙纪念医院 |
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Applicant address: |
Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 Yanjiang West Road, Yuexiu District, Guangzhou City, Guangdong Province |
Study leader's address: |
Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 Yanjiang West Road, Yuexiu District, Guangzhou City, Guangdong Province |
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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: |
中山大学孙逸仙纪念医院 |
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Applicant's institution: |
Sun Yat-sen Memorial Hospital, Sun Yat-sen University |
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研究负责人所在单位: |
中山大学孙逸仙纪念医院 |
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Affiliation of the Leader: |
Sun Yat-sen Memorial Hospital, Sun Yat-sen 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: |
SYSKY-2023-1148-01 |
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: |
中山大学孙逸仙纪念医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee, Sun Yat-sen Memorial Hospital, Sun Yat-sen University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-11-17 00:00:00 | ||
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伦理委员会联系人: |
区柳珊 |
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Contact Name of the ethic committee: |
Ou Liushan |
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伦理委员会联系地址: |
广东省广州市沿江西路107号 |
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Contact Address of the ethic committee: |
107 Yanjiang West Road, Yuexiu District, Guangzhou City, Guangdong Province |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 81332587 |
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: |
中山大学孙逸仙纪念医院 |
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Primary sponsor: |
Sun Yat-sen Memorial Hospital, Sun Yat-sen University |
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研究实施负责(组长)单位地址: |
广东省广州市越秀区沿江西路107号中山大学孙逸仙纪念医院 |
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Primary sponsor's address: |
Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 Yanjiang West Road, Yuexiu District, Guangzhou City, Guangdong Province |
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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: |
广东天普生化医药股份有限公司 |
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Source(s) of funding: |
techpool |
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研究疾病: |
低血容量性休克 |
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Target disease: |
hypovolemic shock |
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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: |
队列研究 |
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Study design: |
Cohort study |
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研究目的: |
主要目的:评估乌司他丁对提高低血容量性休克患者早期复苏效率的疗效。 次要目的:1、评估乌司他丁对低血容量性休克患者(根据严重程度进行分层)临床预后的影响;2、评估乌司他丁对低血容量性休克患者炎症因子的影响;3、评估乌司他丁抗炎治疗策略对低血容量性休克患者多器官功能的影响;4、评估乌司他丁真实世界用药量效关系与安全性。 |
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Objectives of Study: |
Objective: To evaluate the effect of ulinastatin on early resuscitation efficiency in patients with hypovolemic shock. Secondary objectives: 1. To evaluate the effect of ulinastatin on clinical prognosis in patients with hypovolemic shock (stratified according to severity); 2. 2. To evaluate the effect of ulinastatin on inflammatory factors in patients with hypovolemic shock; 3. To evaluate the effect of ulinastatin anti-inflammatory treatment strategy on multiple organ function in patients with hypovolemic shock; 4. Evaluate the dose-effect relationship and safety of ulinastatin in real world use. |
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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)患有自身免疫性疾病(如恶性肿瘤、HIV) (2)1个月内接受过大剂量激素(泼尼松30~100mg/d或等效剂量)、免疫抑制剂治疗的患者 (3)患有严重基础疾病,如慢性肾衰、肝衰竭的患者。 |
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Exclusion criteria: |
(1)Have an autoimmune disease (such as cancer, HIV) (2)Patients who received excessive doses of hormone (prednisone 30-100 mg/ d or equivalent dose) and immunosuppressants within 1 month (3)Patients with serious underlying diseases, such as chronic kidney failure and liver failure |
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研究实施时间: Study execute time: |
从 From 2023-10-01 00:00:00至 To 2025-06-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-01-01 00:00:00 至 To 2025-06-01 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): |
NA |
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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: |
NA |
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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 |
否No |
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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): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
NA |
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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: |
数据录入后,根据 CRF 核查计划的要求内容采用人工检查。核查的内容包括数据的完整性、一致性、逻辑性和方案的违背和偏离等。如纳入排除标准检查、缺失值检查、时间窗检查、逻辑关系检查及实验室检查判断情况检查。如有疑问,可填写数据疑问表,由研究者对疑问表中的问题进行书面解答并签名,交回数据管理员。由数据管理员逐项核对,予以修正确认。上述工作完成后,关闭数据。数据关闭后即可进行数据审核,数据库通过审 核并认为所建立的数据库正确后,将由主要研究者、申办者、统计分析人员和监督管理人员对数据进行锁定。锁定后的数据文件不允许再作变动。数据库将交统计分析人员按统计计划书要求进行统计分析。当数据使用和共享时,需要明确数据使用的目的、方式和范围,并遵守数据共享的相关法律和伦理规定,确保数据的安全和保密。此外,需要明确数据保留期限,并建立相应的数据备份和恢复机制,以保证数据的完整性和可复制性。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
After data entry, manual inspection was performed according to the requirements of the CRF verification plan. The content of verification included data integrity, consistency, logic and protocol violation and deviation. Such as inclusion and exclusion criteria check, missing value check, time window check, logical relationship check and laboratory test judgment check. In case of doubt, the data query form was completed, and the questions in the query form were answered in writing and signed by the investigator and returned to the data manager. The data manager shall check item by item and revise and confirm. After the above work was completed, the data were closed. After the data is closed, the data review can be carried out, and the database is approved The data were locked by the principal investigators, sponsor, statistical analysts, and regulatory staff after the database was verified and deemed to be correct. The locked data file is not allowed to change. The database will be submitted to the statistical analyst for statistical analysis as required in the statistical plan. When data is used and shared, it is necessary to clarify the purpose, method and scope of data use, comply with relevant legal and ethical regulations on data sharing, and ensure data security and confidentiality. In addition, it is necessary to clarify the data retention period and establish the corresponding data backup and recovery mechanism to ensure the integrity and replicability of the data. |
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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 |