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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: |
ChiCTR-TRC-12002562 |
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最近更新日期: Date of Last Refreshed on: |
2015-10-29 14:20:43 |
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注册时间: Date of Registration: |
2012-06-26 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: |
比较JUC长效抗微生物材料与安慰剂预防急性尿潴留患者导尿管伴随性尿路感染的随机双盲试验 |
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Public title: |
Comparing JUC long term anti-microbial material to placebo for prevention of catheter with urinary tract infection in acute urinary retention patients: a randomized, double blinded, controlled 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: |
比较JUC长效抗微生物材料与安慰剂预防急性尿潴留患者导尿管伴随性尿路感染的随机双盲试验 |
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Scientific title: |
Comparing JUC long term anti-microbial material to placebo for prevention of catheter with urinary tract infection in acute urinary retention patients: a randomized, double blinded, controlled 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: |
梁萍 |
研究负责人: |
叶章群 |
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Applicant: |
Liang Ping |
Study leader: |
Ye Zhangqun |
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申请注册联系人电话: Applicant telephone: |
+86 025 83400310-810 |
研究负责人电话:
Study leader's |
+86 13507191761 |
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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: |
nms@juc365.com |
研究负责人电子邮件: Study leader's E-mail: |
zhangqun_ye@yahoo.com.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: |
江苏省南京市鼓楼区山西路128号1701室 |
研究负责人通讯地址: |
湖北省武汉市解放大道1095号 |
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Applicant address: |
Rm. 1701, 128 Shanxi Road, Gulou District, Nanjing, Jiangshu |
Study leader's address: |
1095 Jiefang Road, Wuhan, China |
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申请注册联系人邮政编码: Applicant postcode: |
210009 |
研究负责人邮政编码: Study leader's postcode: |
430030 |
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申请人所在单位: |
中华医学会泌尿外科学分会 |
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Applicant's institution: |
The Chinese Medical Association Urinary Surgery Branch |
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研究负责人所在单位: |
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Affiliation of the Leader: |
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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: |
ChiECRCT-2012021 |
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: |
中国注册临床试验伦理审查委员会 |
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Name of the ethic committee: |
Chinese Ethicc Committee of Registering Clinical Trials |
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伦理委员会批准日期: Date of approved by ethic committee: |
2012-09-23 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: |
华中科技大学同济医学院附属同济医院 |
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Primary sponsor: |
Tongji Hospital Affiliated to Tongji Medical School, Huazhong Science and Technical University |
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研究实施负责(组长)单位地址: |
湖北省武汉市解放大道1095号 |
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Primary sponsor's address: |
1095 Jiefang Road, Wuhan, 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: |
由JUC生产厂家赞助研究用试剂 |
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Source(s) of funding: |
The manufactor provides the agents |
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研究疾病: |
急性尿潴留患者留置导尿管伴随性尿路感染 |
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Target disease: |
Indwelling catheter concomitant urinary tract infection in acute urinary retention patients |
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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: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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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: |
本研究旨在将JUC喷洒在导尿管表面,在体内阻止BF形成的效果,以及不采用抗生素的前提下,降低急性尿潴留患者导尿期间CAUTI的发生率。 |
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Objectives of Study: |
This study aims to determine the effect of apply JUC on the surface of catheter to stop forms of the BF, as well as reducing the rate of concomitant urinary tract infection during catheterize urine by indwelling the catheter in the acute urinary retention 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: |
50-80周岁的急性尿潴留患者,要求植入气囊式导尿管的患者;上述纳入标准必须同时满足,才能入选。 |
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Inclusion criteria |
1. aged 50~80 years old; |
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排除标准: |
1)体温>38.5℃;2)每高倍镜视野白细胞>5个;3)需要14天以上治疗的顽固性感染;4)两周内使用过导尿管;5)自我间歇导尿患者;6)有耻骨上/经皮肾穿刺造瘘术者;7)7-14天内接受抗生素治疗者;8)有精神系统疾病;9)其他免疫抑制性疾病;上述排除标准,有一项符合即被排除。 |
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Exclusion criteria: |
1. Patients with fever, the temparature higher than 38.5 degree C; |
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研究实施时间: Study execute time: |
从 From 2012-10-08 00:00:00至 To 2013-01-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2012-10-08 00:00:00 至 To 2012-10-31 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: |
结束 /Completed |
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): |
受试者随机选择,研究采用双盲试验方法。 JUC长效抗微生物材料和安慰剂采用同样的包装,所有试验试剂在外观和气味上应该一致,将同样数量的JUC长效抗微生物材料和安慰剂按照随机数表进行标号,具体编号信息 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Random number table will be used to generate an allocation sequence by the statistician. |
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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: |
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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 |
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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): |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
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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: |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |