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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: |
ChiCTR2000036894 |
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最近更新日期: Date of Last Refreshed on: |
2020-09-21 00:07:21 |
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注册时间: Date of Registration: |
2020-08-25 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: |
三类医疗器械自动化局部枸橼酸抗凝仪的注册前临床验证 |
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Public title: |
Clinical verification of automatic local citrate anticoagulant apparatus before registration |
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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: |
三类医疗器械自动化局部枸橼酸抗凝仪的注册前临床验证 |
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Scientific title: |
Clinical verification of automatic local citrate anticoagulant apparatus before registrat |
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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: |
毕逍 |
研究负责人: |
丁峰 |
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Applicant: |
Xiao Bi |
Study leader: |
Feng Ding |
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申请注册联系人电话: Applicant telephone: |
+86 13917040554 |
研究负责人电话: Study leader's telephone: |
+86 18919790062 |
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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: |
bixiao0305@163.com |
研究负责人电子邮件: Study leader's E-mail: |
dingfeng@sjtu.edu.cn |
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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: |
上海市黄浦区制造局路639号 |
研究负责人通讯地址: |
上海市黄浦区制造局路639号 |
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Applicant address: |
639 Zhizaoju Road, Huangpu District, Shanghai, China |
Study leader's address: |
639 Zhizaoju Road, Shanghai, China |
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申请注册联系人邮政编码: Applicant postcode: |
200011 |
研究负责人邮政编码: Study leader's postcode: |
200011 |
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申请人所在单位: |
上海交通大学医学院附属第九人民医院 |
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Applicant's institution: |
Ninth People's Hospital affiliated to Shanghai Jiaotong University School of Medicine |
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研究负责人所在单位: |
上海交通大学医学院附属第九人民医院 |
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Affiliation of the Leader: |
Ninth People's Hospital affiliated to Shanghai Jiaotong University School of 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: |
SH9H-2020-T263-2 |
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: |
上海交通大学医学院附属第九人民医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Ninth People's Hospital affiliated to Shanghai Jiaotong University School of Medicine |
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伦理委员会批准日期: Date of approved by ethic committee: |
2020-08-21 00:00:00 |
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伦理委员会联系人: |
姚敏 |
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Contact Name of the ethic committee: |
Min Yao |
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伦理委员会联系地址: |
上海市黄浦区制造局路639号 |
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Contact Address of the ethic committee: |
639 Zhizaoju Road, Huangpu District, Shanghai, 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: |
上海交通大学医学院附属第九人民医院 |
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Primary sponsor: |
Ninth People's Hospital affiliated to Shanghai Jiaotong University School of Medicine |
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研究实施负责(组长)单位地址: |
上海市黄浦区制造局路639号 |
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Primary sponsor's address: |
639 Zhizaoju Road, Huangpu District, Shanghai, 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: |
上海市申康项目 |
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Source(s) of funding: |
Shenkang Project |
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Target disease: |
Chronic kidney disease |
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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: |
探索性研究/预试验 | ||||||||||||||||||||||
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Study phase: |
0 |
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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: |
拟进行双中心、随机、开放、对照研究,比较自动化RCA仪的核心算法“二阶段补钙法”和目前临床上广泛使用的传统试错法的抗凝效果和安全性。 |
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Objectives of Study: |
We aim to conduct RCT study to compare our two-phase calcium supplementation model with the conventional trial |
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药物成份或治疗方案详述: |
1) 采用股静脉或颈内静脉临时置管建立血管通路。 2) CRRT机型及滤器不限,每72h更换滤器。 3) 根据KDIGO指南,CRRT剂量最低为设为25 ml/kg/h。为避免模式及治疗剂量单一,采用CVVHD或CVVHDF透析模式,治疗时间根据患者病情需要分为8-12h或≥24h。进行8-12h RCA-CRRT的患者CVVHD模式可设置血流量180-200ml/min,进行超过24h RCA-CRRT的患者可设置血流量100-150ml/min。置换液及透析液流速见下图。 4) 透析液及置换液标准含Na+ 133mmol/L,K+ 2mmol/L,Ca2+ 0 mmol/L,Mg2+ 0.75mmol/L,Cl- 116.5mmol/L,葡萄糖1g/L,HCO3- 20mmol/l。 5) 循环管路动脉段采用血液保存液ACD-A(枸橼酸钠22g/L,枸橼酸8g/L)进行枸橼酸抗凝,静脉段补充1%氯化钙。两组均使用精准输液泵及输注泵。 6) 传统试错法由中心根据以往RCA经验给予起始钙和枸橼酸输注速度,根据体内和体外循环离子钙水平调整输注速度。“二阶段补钙法”通过输入患者血流量、红细胞压积、透析液流量、超滤量、体重、血总钙水平,计算枸橼酸及1%氯化钙用量。 |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
1)急性肾损伤合并严重高钾血症、代谢性酸中毒(K+ > 6.5mmol/L,PH < 7.25); 2)利尿剂无法纠正的高容量; 3)高分解代谢:血清肌酐和尿素氮持续上升; 4)合并多器官功能障碍; |
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Inclusion criteria |
1 Acute kidney injury with hyperkalemia or metabolic acidosis 2 Volume overload irreversible with diuretic 3 Hypercatabolic 4 MODS |
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排除标准: |
1)72h内使用过含枸橼酸药品或制剂; 2)同时已纳入其余临床试验; 3)无法建立血流量稳定的血管通路; 4)预计生存时间短于72小时; |
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Exclusion criteria: |
1 Application of drugs containing citrate within 72h 2 Engagement in other clinical trial 3 Failure to establish vessel access |
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研究实施时间: Study execute time: |
从 From 2020-10-01 00:00:00至 To 2022-09-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 1990-01-01 00:00:00 至 To 1990-01-01 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: |
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): |
使用随机分配表进行分配 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Random assignment table |
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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: |
数据分析人员不知道患者分组 |
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Blinding: |
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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): |
2023.3 网络平台 http://www.chictr.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): |
2023.3 web-based public database http://www.chictr.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: |
病例记录表 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Record Form |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |