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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: |
ChiCTR1800014464 |
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最近更新日期: Date of Last Refreshed on: |
2020-01-05 18:31:50 |
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注册时间: Date of Registration: |
2018-01-16 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: |
马晓冉医师:该研究的伦理审批文件未上传,请尽快上传。 氟比洛芬酯术后镇痛对高血压患者肾功能的影响 |
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Public title: |
Effect of flurbiprofen axetil on renal function as postoperative analgesic in hypertensive patients |
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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: |
氟比洛芬酯术后镇痛对高血压患者肾功能的影响 |
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Scientific title: |
Effect of flurbiprofen axetil on renal function as postoperative analgesic in hypertensive patients |
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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: |
马晓冉 |
研究负责人: |
冯艺 |
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Applicant: |
Ma Xiaoran |
Study leader: |
Feng Yi |
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申请注册联系人电话: Applicant telephone: |
+86 18210200996 |
研究负责人电话: Study leader's telephone: |
+86 13331086387 |
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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: |
374299701@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
yifeng65@sina.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: |
北京市西城区西直门南大街11号 |
研究负责人通讯地址: |
北京市西城区西直门南大街11号 |
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Applicant address: |
11 Xizhimen Street South, Xicheng District, Beijing, China |
Study leader's address: |
11 Xizhimen Street South, Xicheng District, Beijing, China |
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申请注册联系人邮政编码: Applicant postcode: |
100044 |
研究负责人邮政编码: Study leader's postcode: |
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申请人所在单位: |
北京大学人民医院 |
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Applicant's institution: |
Peking University People's Hospital |
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研究负责人所在单位: |
北京大学人民医院 |
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Affiliation of the Leader: |
Peking University People's Hospital |
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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: |
2016PHB147-01 |
伦理委员会批件附件: Approved file of Ethical Committee: |
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批准本研究的伦理委员会名称: |
北京大学人民医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Peking University People's Hospital. |
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伦理委员会批准日期: Date of approved by ethic committee: |
2016-11-16 00:00:00 |
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伦理委员会联系人: |
丛翠翠 |
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Contact Name of the ethic committee: |
CongCuicui |
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伦理委员会联系地址: |
北京市西城区西直门南大街11号 |
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Contact Address of the ethic committee: |
11 Xizhimen Street South, Xicheng District, Beijing, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 010-88324516 |
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: |
北京大学人民医院 |
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Primary sponsor: |
Peking University People's Hospital |
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研究实施负责(组长)单位地址: |
北京市西城区西直门南大街11号 |
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Primary sponsor's address: |
11 Xizhimen Street South, Xicheng District, Beijing, 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: |
吴阶平医学基金会临床科研专项资助基金 |
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Source(s) of funding: |
Wu Jieping Medical Funds of Clinical Research |
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Target disease: |
Hypertension |
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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: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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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: |
探讨氟比洛芬酯术后静脉镇痛对高血压患者肾脏功能的影响。 |
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Objectives of Study: |
To investigate the effect of flurbiprofen axetil on renal function as postoperative analgesic in hypertensive patients. |
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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: |
拟行膝关节置换术患者60例,ASAⅠ或Ⅱ级,按照是否合并高血压分为H组(合并高血压病患者)和C组(血压正常患者),每组30人。 |
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Inclusion criteria |
60 patients that will undergo total knee replacement surgery, ASA I or II grade; According to whether the patients suffer from hypertension, 60 patients will be divided into H group (patients with hypertension) and group C (patients with normal blood pressure), 30 patients in each group. |
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排除标准: |
1.已知对氟比洛芬酯过敏的患者。2.服用阿司匹林或其他非甾体类抗炎药后诱发哮喘、荨麻疹或过敏反应的患者。3.有应用非甾体抗炎药后发生胃肠道出血或穿孔病史的患者。4.有活动性消化道溃疡/出血,或者既往曾复发溃疡/出血的患者。5.重度心力衰竭患者。6.肝、肾及血液系统功能障碍患者。7.正在使用依诺沙星、洛美沙星、诺氟沙星的患者。 |
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Exclusion criteria: |
1. Patients who are known to be allergic to flurbiprofen; |
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研究实施时间: Study execute time: |
从 From 2018-02-01 00:00:00至 To 2018-05-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2018-02-01 00:00:00 至 To 2018-05-31 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): |
由不清楚具体试验方案的第三方根据随机数字表进行患者随机化入组。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Patients are randomly assigned to the group according to the random digital table by the third party who do not know the specific study plan. |
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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 |
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): |
Resman临床试验公共管理平台 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Resman clinical trial public management platform,www.medresman.org |
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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: |
数据采集应用病例记录表,数据管理采用Resman临床试验公共管理平台。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Use case record form for data collection and use ResMan for data management. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |