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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: |
ChiCTR1800016087 |
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最近更新日期: Date of Last Refreshed on: |
2022-03-23 07:29:52 |
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注册时间: Date of Registration: |
2018-05-10 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
摩罗丹治疗慢性萎缩性胃炎随机、双盲、平行对照、多中心临床试验 |
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Public title: |
The treatment of chronic atrophic gastritis by Moluodan: a randomized, double-blind, parallel controlled, multicenter 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: |
摩罗丹治疗慢性萎缩性胃炎随机、双盲、平行对照、多中心临床试验 |
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Scientific title: |
The treatment of chronic atrophic gastritis by Moluodan: a randomized, double-blind, parallel controlled, multicenter 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: |
杨萌 |
研究负责人: |
房静远 |
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Applicant: |
Meng Yang |
Study leader: |
Jingyuan Fang |
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申请注册联系人电话: Applicant telephone: |
+86 15712804601 |
研究负责人电话:
Study leader's |
+86 13918386561 |
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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: |
yangmeng@hanyao.com.cn |
研究负责人电子邮件: Study leader's E-mail: |
13046678061@163.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: |
北京市石景山区鲁谷路74号瑞达大厦M701 |
研究负责人通讯地址: |
上海市黄埔区山东中路145号 |
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Applicant address: |
Room M701, Ruida Building, 74 Lugu Road, Shijingshan District, Beijing, China |
Study leader's address: |
145 Shandong Road, Whampoa District, Shanghai |
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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: |
邯郸制药股份有限公司 |
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Applicant's institution: |
Handan Pharmaceutical Co.,Ltd. |
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研究负责人所在单位: |
上海交通大学医学院附属仁济医院 |
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Affiliation of the Leader: |
Shanghai Jiaotong University School of Medicine, Renji Hospital |
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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: |
2017-064 |
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仁济医院医学伦理委员会 |
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Name of the ethic committee: |
Shanghai Jiaotong University School of Medicine, Renji Hospital Ethics Committee |
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伦理委员会批准日期: Date of approved by ethic committee: |
2017-08-30 00:00:00 | ||
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伦理委员会联系人: |
陆麟 |
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Contact Name of the ethic committee: |
Lin Lu |
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伦理委员会联系地址: |
上海市浦建路160号 |
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Contact Address of the ethic committee: |
160 Pujian Road, 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仁济医院 |
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Primary sponsor: |
Renji Hospital, Shanghai Jiaotong University School of Medicine |
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研究实施负责(组长)单位地址: |
上海市黄埔区山东中路145号 |
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Primary sponsor's address: |
145 Shandong Road, Whampoa District, Shanghai |
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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: |
邯郸制药股份有限公司 |
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Source(s) of funding: |
Handan Pharmaceutical Co.,Ltd. |
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研究疾病: |
慢性萎缩性胃炎 |
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Target disease: |
chronic atrophic gastritis |
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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: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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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: |
评价摩罗丹治疗慢性萎缩性胃炎的有效性及临床应用的安全性 |
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Objectives of Study: |
To evaluate the efficacy and safety of Moluodan in the treatment of chronic atrophic gastritis |
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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: |
1.年龄为18~70岁,性别不限; |
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Inclusion criteria |
1. Aged between 18-70 years old, male or female; |
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排除标准: |
1.合并消化性溃疡、胃粘膜有中度或者重度异型增生或病理诊断疑有恶病变者; |
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Exclusion criteria: |
1. Combined with peptic ulcer, moderate or severe dysplasia of gastric mucosa or pathological diagnosis of suspected malignant change; |
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研究实施时间: Study execute time: |
从 From 2017-09-30 00:00:00至 To 2022-03-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2017-11-03 00:00:00 至 To 2019-12-31 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: |
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): |
用于药物随机编盲的随机数字表由统计学专业人员提供,利用SAS9.4(或更高)软件固定种子数产。并由与本次临床研究无关人员完成药物编盲及应急信件的准备工作,其中药物经随机编盲后的药物编号即为随机号。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
A random number table for drug random blindness is provided by statistical professionals, using SAS9.4 (or higher) software to fix seed numbers. The preparation of drug blindness and emergency correspondence was completed by people who were not related to this clinical study. The drug number was random number |
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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: |
Not stated |
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Blinding: |
Not stated |
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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 |
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): |
中国临床试验注册中心 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
China Clinical Laboratory Registration Center |
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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: |
本试验病历记录表由试验负责人和试验小组研究人员共同设计。所有受试者纸质版资料均存放在医院限制区内安全锁定的文件柜中,只有试验相关研究人员可查阅。所有受试者电子版资料将录入需要密码登录的安全的数据库中,只有实验相关人员可登录。所有试验相关数据在试验完成后至少保留五年。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
The case record form is designed by study leader and study team researchers.The paper version data of all subjects will be locked in the restricted area of hospital safely,and only test-related researchers can refer to.The electronic version data of all subjects will be entered in a password required secure database,and only lab-related personnel can log in.All test-related data will be kept for at least five years after the test is completed. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |