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注册号: Registration number: |
ChiCTR2100048745 |
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最近更新日期: Date of Last Refreshed on: |
2022-03-26 03:46:45 |
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注册时间: Date of Registration: |
2021-07-15 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: |
oXiris与常规CRRT治疗早期重症胰腺炎腹腔高压的多中心随机对照临床试验 |
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Public title: |
oXiris versus conventional CRRT in the treatment of early severe pancreatitis with abdominal hypertension: a multicenter randomized controlled clinical trial |
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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: |
oXiris与常规CRRT治疗早期重症胰腺炎腹腔高压的多中心随机对照临床试验 |
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Scientific title: |
oXiris versus conventional CRRT in the treatment of early severe pancreatitis with abdominal hypertension: a multicenter randomized controlled clinical trial |
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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: |
胡丽丽 |
研究负责人: |
刘勇 |
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Applicant: |
Hu Lili |
Study leader: |
Liu Yong |
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申请注册联系人电话: Applicant telephone: |
+86 13502813771 |
研究负责人电话:
Study leader's |
+86 13928415176 |
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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: |
317001977@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
liuyongjoy@outlook.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: |
广东深圳市宝安区新湖路1333号 |
研究负责人通讯地址: |
广东深圳市宝安区新湖路1333号 |
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Applicant address: |
1333 Xinhu Road, Bao'an District, Shenzhen, Guangdong |
Study leader's address: |
1333 Xinhu Road, Bao'an District, Shenzhen, Guangdong |
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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: |
南方医科大学深圳医院 |
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Applicant's institution: |
Shenzhen Hospital, Southern Medical University |
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研究负责人所在单位: |
南方医科大学深圳医院 |
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Affiliation of the Leader: |
Shenzhen Hospital, Southern Medical 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: |
NYSZYYEC20210012 |
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: |
南方医科大学深圳医院医学伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Shenzhen Hospital, Southern Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2021-07-05 00:00:00 | ||
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伦理委员会联系人: |
陈烨 |
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Contact Name of the ethic committee: |
Chen Ye |
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伦理委员会联系地址: |
广东深圳市宝安区新湖路1333号 |
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Contact Address of the ethic committee: |
1333 Xinhu Road, Bao'an District, Shenzhen, Guangdong |
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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: |
南方医科大学深圳医院 |
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Primary sponsor: |
Shenzhen Hospital, Southern Medical University |
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研究实施负责(组长)单位地址: |
广东深圳市宝安区新湖路1333号 |
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Primary sponsor's address: |
1333 Xinhu Road, Bao'an District, Shenzhen, Guangdong |
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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: |
南方医科大学深圳医院 |
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Source(s) of funding: |
Shenzhen Hospital, Southern Medical University |
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研究疾病: |
早期重症胰腺炎腹腔高压 |
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Target disease: |
early severe pancreatitis with abdominal hypertension |
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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: |
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: |
评估oXiris滤器治疗对重症胰腺炎并发腹腔高压的干预效果。 |
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Objectives of Study: |
To evaluate the intervention effect of oXiris filter treatment on severe pancreatitis complicated with abdominal hypertension. |
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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.若研究过程中出现明显循环衰竭,经医院相关专家会诊讨论后决定是否改方案,并与患者及家属沟通最佳方案,如患者和/或家属仍要求退出则可退出该研究; |
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Exclusion criteria: |
1. If there is obvious circulatory failure during the study, after consultation and discussion with relevant experts in the hospital, decide whether to change the plan, and communicate with the patients and their families about the best plan. If the patients and/or family members still request to withdraw, they can withdraw from the study; |
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研究实施时间: Study execute time: |
从 From 2021-09-01 00:00:00至 To 2025-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2021-09-01 00:00:00 至 To 2025-12-31 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: |
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): |
使用基于网络的软件(www.randomizer.org)以1:1的比率生成随机序列,以确定分组(实验组或对照组)。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Use web-based software (www.randomizer.org) to generate random sequences at a ratio of 1:1 to determine the grouping (experimental group or control group). |
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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: |
Not stated |
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Blinding: |
Not stated |
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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): |
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): |
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: |
CRF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 Report Form |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |