|
审核状态: Project audit state: |
通过审核 Successful |
|
注册号: Registration number: |
ChiCTR2100043457 |
|
最近更新日期: Date of Last Refreshed on: |
2021-02-19 02:50:59 |
|
注册时间: Date of Registration: |
2021-02-19 00:00:00 |
|
注册号状态: |
补注册 |
|
Registration Status: |
Retrospective registration |
|
注册题目: |
多中心、随机、双盲双模拟、阳性药平行对照的Ⅲ期临床研究评价H008片用于十二指肠溃疡患者的有效性和安全性 |
|
Public title: |
A multi-center, randomized, double-blind, double-simulated, and positive-drug parallel-controlled Phase III clinical study to evaluate the effectiveness and safety of H008 tablets in patients with duodenal ulcer |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
多中心、随机、双盲双模拟、阳性药平行对照的Ⅲ期临床研究评价H008片用于十二指肠溃疡患者的有效性和安全性 |
|
Scientific title: |
A multi-center, randomized, double-blind, double-simulated, and positive-drug parallel-controlled Phase III clinical study to evaluate the effectiveness and safety of H008 tablets in patients with duodenal ulcer |
|
研究课题代号(代码): Study subject ID: |
|
|
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: |
|
申请注册联系人: |
夏珏妤 |
研究负责人: |
陈旻湖、肖英莲 |
|
Applicant: |
Jueyu Xia |
Study leader: |
Minhu Chen、Yinglian Xiao |
|
申请注册联系人电话: Applicant telephone: |
+86 15805195658 |
研究负责人电话:
Study leader's |
+86 020-87755766-8189 |
|
申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
||
|
申请注册联系人电子邮件: Applicant E-mail: |
xiajueyu@kfpyy.com |
研究负责人电子邮件: Study leader's E-mail: |
chenminhu@mail.sysu.edc.cn |
|
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): |
||
|
申请注册联系人通讯地址: |
江苏省南京市玄武区徐庄路6号1幢 |
研究负责人通讯地址: |
广东省广州市中山二路58号 |
|
Applicant address: |
Building 1, 6 Xuzhuang Road, Nanjing, Jiangsu |
Study leader's address: |
58 Second Zhongshan Road, Guangzhou, Guangdong |
|
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: |
||
|
申请人所在单位: |
江苏柯菲平医药股份有限公司 |
||
|
Applicant's institution: |
Jiangsu Carephar Pharmaceutical Co., Ltd. |
||
|
研究负责人所在单位: |
中山大学附属第一医院 |
||
|
Affiliation of the Leader: |
the First Affiliated Hospital of Sun Yat-sen University |
||
|
是否获伦理委员会批准: |
是 |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
2020-039-01、2020-039-02 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
|
批准本研究的伦理委员会名称: |
中山大学附属第一医院临床药品、设备和医疗新技术伦理委员会 |
||
|
Name of the ethic committee: |
The Ethics Committee of the First Affiliated Hospital of Sun Yat-sen University |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
1990-01-01 00:00:00 | ||
|
伦理委员会联系人: |
林颖 |
||
|
Contact Name of the ethic committee: |
Ying Lin |
||
|
伦理委员会联系地址: |
广东省广州市竹丝岗二马路5号龙珠大厦写字楼1楼110房 |
||
|
Contact Address of the ethic committee: |
Room 110, 1st Floor, Longzhu Building, 5 Zhusigang 2nd Road, Guangzhou,Guangdong |
||
|
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: |
||
|
研究实施负责(组长)单位: |
中山大学附属第一医院 |
||||||||||||||||||||||
|
Primary sponsor: |
The First Affiliated Hospital of Sun Yat-sen University |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
广东省广州市中山二路58号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
58 Zhongshan 2nd Road, Guangzhou, Guangdong |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
江苏柯菲平医药股份有限公司 |
||||||||||||||||||||||
|
Source(s) of funding: |
Jiangsu Carephar Pharmaceutical Co., Ltd. |
||||||||||||||||||||||
|
研究疾病: |
十二指肠溃疡 |
||||||||||||||||||||||
|
Target disease: |
Duodenal ulcer |
||||||||||||||||||||||
|
研究疾病代码: |
|
||||||||||||||||||||||
|
Target disease code: |
|
||||||||||||||||||||||
|
研究类型: |
干预性研究 |
||||||||||||||||||||||
|
Study type: |
Interventional study |
||||||||||||||||||||||
|
研究所处阶段: |
III期临床试验 | ||||||||||||||||||||||
|
Study phase: |
3 |
||||||||||||||||||||||
|
研究设计: |
随机平行对照 |
||||||||||||||||||||||
|
Study design: |
Parallel |
||||||||||||||||||||||
|
研究目的: |
主要目的: 1)与兰索拉唑肠溶胶囊相比,评价H008片治疗十二指肠溃疡的有效性; 次要目的: 1)与兰索拉唑肠溶胶囊相比,评价H008片治疗十二指肠溃疡的安全性; 2)观察H008片在十二指肠溃疡患者中的群体药代动力学特征; 3)观察H008片用于十二指肠溃疡患者后血清胃泌素的治疗前后变化情况。 |
||||||||||||||||||||||
|
Objectives of Study: |
The primary purpose: 1) Compared with lansoprazole enteric-coated capsules, evaluate the effectiveness of H008 tablets in the treatment of duodenal ulcer; The secondary purpose: 1) Compared with lansoprazole enteric-coated capsules, evaluate the safety of H008 tablets in the treatment of duodenal ulcer; 2) Observe the populational pharmacokinetic characteristics of H008 tablets in patients with duodenal ulcer; 3) Observe the changes of serum gastrin before and after treatment with H008 tablets in patients with duodenal ulcer. |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
|
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||
|
纳入标准: |
1)18周岁≤年龄≤75周岁,性别不限; |
||||||||||||||||||||||
|
Inclusion criteria |
1) 18 years old ≤ age ≤ 75 years old, no gender limit; |
||||||||||||||||||||||
|
排除标准: |
1)既往接受过H008片给药者; |
||||||||||||||||||||||
|
Exclusion criteria: |
1) Those who have received H008 tablets in the past; |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2020-07-10 00:00:00至 To 2021-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2020-08-21 00:00:00 至 To 2021-01-04 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
正在进行 Recruiting |
年龄范围: Participant age: |
|
||||||
|
性别: |
男女均可 |
Gender: |
Both |
||||||
|
随机方法(请说明由何人用什么方法产生随机序列): |
本次试验使用双盲双模拟技术,即研究者、受试者及参与试验的其他方均不能确定受试者服用的是何种药物。试验组使用的H008片与模拟剂、对照组使用的兰索拉唑肠溶胶囊与模拟剂均由江苏柯菲平医药股份有限公司提供。试验药物与试验药物模拟剂、对照药品与对照药品模拟剂在外观、形状、规格用量等方面基本相同。 药物包装由随机化统计师和与本试验无关的人员参加,并对整个编盲过程进行详细记录。编盲完成后,随机化统计师对盲底进行封存,并移交申办方或合同研究组织项目经理;盲底一式两份分别封存在申办者和临床研究负责单位机构办公室。在研究中研究医生和受试者均不知道治疗期使用的H008片还是对照药品以达到双盲要求。 由于本试验各试验组与对照组样本比例1:1,故采用两级揭盲方法。当数据全部输入数据库后,经盲态审核、数据库锁定、统计分析计划书确定后执行第一次揭盲,确定病例归属到试验组别A组或B组,交由统计人员进行统计分析。统计分析主要结果分析完成后进行二次揭盲,以确定A组或B组对应的是试验组或对照组。揭盲过程由主要研究者、统计单位、申办单位或其代表共同完成,且揭盲过程均应有相应的记录。 因发生严重不良事件或其他紧急情况下 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
Stratified randomization |
||||||||
|
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 |
|
盲法: |
|
|
Blinding: |
|
是否共享原始数据: IPD sharing |
是Yes |
|
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): |
EDC,百奥知,https://ktp.bioknow.net/edc_cts_co_2002_pro |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
EDC,Bioknow,https://ktp.bioknow.net/edc_cts_co_2002_pro |
|
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: |
数据录入EDC系统 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
All required date were written into EDC |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |