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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-13004069 |
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最近更新日期: Date of Last Refreshed on: |
2015-05-05 12:44:32 |
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注册时间: Date of Registration: |
2013-04-10 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: |
苦丁香通气栓III期临床研究 |
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Public title: |
Phase III Clinical Trial of Kudingxiang Tong Qi Suppository |
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注册题目简写: |
苦丁香通气栓 |
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English Acronym: |
TQS |
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研究课题的正式科学名称: |
苦丁香通气栓治疗腹部手术后肠麻痹有效性及安全性的随机、双盲、安慰剂平行对照、多中心临床试验 |
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Scientific title: |
A randomized, double blinded, placebo controlled, parallel grouped, multi-centre clinical study on safety and efficacy of TQS for restoring gastrointestinal function after abdominal surgery |
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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: |
2009L01190 |
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申请注册联系人: |
谢忱 |
研究负责人: |
谢忱 |
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Applicant: |
Chen Xie |
Study leader: |
Chen Xie |
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申请注册联系人电话: Applicant telephone: |
+86 13501261306 |
研究负责人电话:
Study leader's |
+86 13501261306 |
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申请注册联系人传真 : Applicant Fax: |
+86-10-80729874 |
研究负责人传真: Study leader's fax: |
+86-10-80729874 |
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申请注册联系人电子邮件: Applicant E-mail: |
cxie@botaniccentury.com |
研究负责人电子邮件: Study leader's E-mail: |
cxie@botaniccentury.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
www.snykpharma.com |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
www.snykpharma.com |
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申请注册联系人通讯地址: |
北京市海淀区开拓路5号A-401 |
研究负责人通讯地址: |
北京市海淀区开拓路5号A-401 |
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Applicant address: |
A-401, 5, KaiTuo Road, Haidian District, Beijing, China |
Study leader's address: |
A-401, 5 Kai Tuo Road, Haidian District, Beijing, China |
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申请注册联系人邮政编码: Applicant postcode: |
100085 |
研究负责人邮政编码: Study leader's postcode: |
100085 |
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申请人所在单位: |
北京神农益康医药技术有限公司 |
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Applicant's institution: |
Beijing SNYK Pharmaceutical Ltd |
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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: |
E2012]伦审药临字第(28)号 |
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: |
The Medical Ethics Committee of Renmin Hospital, Bejing University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2011-09-05 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: |
北京大学人民医院 |
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Primary sponsor: |
Renmin Hospital of Beijing University |
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研究实施负责(组长)单位地址: |
北京市西城区阜成门内大街133号 |
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Primary sponsor's address: |
133 FuChengMenNei Street, 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: |
北京神农益康医药技术有限公司 |
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Source(s) of funding: |
Funded by SNYK Pharmaceutical Ltd |
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研究疾病: |
手术后肠麻痹 |
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Target disease: |
Post Operative Illes |
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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: |
III期临床试验 | ||
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Study phase: |
3 |
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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: |
在Ⅱb期基础上,确证苦丁香通气栓治疗腹部手术后肠麻痹的有效性及安全性,为注册审查提供依据。 |
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Objectives of Study: |
Based on Phase IIb clinical trial, to further investigate the efficacy and safety of TQS on restoring gastrointestinal function after abdominal surgery, and to provide the evidence for New drug Application. |
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药物成份或治疗方案详述: |
苦丁香,槟榔 |
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Description for medicine or protocol of treatment in detail: |
Muskmelon-Base and Arecae semen Extract |
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纳入标准: |
⑴ 开腹胃肠道手术患者; |
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Inclusion criteria |
(1)Open abdominal gastrointestinal surgery;(2)Surgery with general anesthesia, and intravenous analgesia after surgey;(3)Aged 18~75;(4)Volantarily to sign the informed consent file. |
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排除标准: |
⑴ 行直肠吻合术的患者;或肠道皮肤造瘘者; |
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Exclusion criteria: |
(1)Patients under rectal anastomosis or intestinal fistulation; |
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研究实施时间: Study execute time: |
从 From 2012-09-05 00:00:00至 To 2014-06-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2012-09-05 00:00:00 至 To 2014-06-16 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): |
采用分层区组随机化方法。由统计师按中心进行分层,选取合适段长。借助SAS统计软件,给定种子数,产生440例(试验组和安慰剂组)受试者所接受处理的随机安排,列出流水号为001~440所对应的治疗分配(即 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
A stratified blocked randomisation method was applied. Stratification was based on centres and prope |
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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: |
双盲法 |
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Blinding: |
Double-blind |
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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: |