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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: |
ChiCTR2300068489 |
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最近更新日期: Date of Last Refreshed on: |
2023-02-21 11:31:21 |
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注册时间: Date of Registration: |
2023-02-21 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: |
得必泰治疗功能性消化不良患者的随机、双盲、安慰剂、平行对照、优效性多中心临床研究 |
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Public title: |
A randomized, double-blind, placebo-controlled, parallel-controlled, superiority multicenter clinical study of Debitai in patients with functional dyspepsia |
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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: |
得必泰治疗功能性消化不良患者的随机、双盲、安慰剂、平行对照、优效性多中心临床研究 |
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Scientific title: |
A randomized, double-blind, placebo-controlled, parallel-controlled, superiority multicenter clinical study of Debitai in patients with functional dyspepsia |
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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: |
钟鸣 |
研究负责人: |
李兆申 |
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Applicant: |
Ming ZHONG |
Study leader: |
Zhao shen LI |
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申请注册联系人电话: Applicant telephone: |
+86 13681961124 |
研究负责人电话: Study leader's telephone: |
+86 13801993592 |
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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: |
zhongming@mylion.com.cn |
研究负责人电子邮件: Study leader's E-mail: |
duyiqi@hotmail.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: |
上海市宝山区友谊西路101号上海建科园3号楼2206室 |
研究负责人通讯地址: |
上海市杨浦区长海路168号,11号楼18层 |
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Applicant address: |
Room 2206, Building 3, Shanghai Jianke Park, 101 Youyi West Road, Baoshan District, Shanghai |
Study leader's address: |
168 Changhai Road, Yangpu District, Shanghai, China |
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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: |
上海迈兰医药咨询有限公司 |
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Applicant's institution: |
SHANGHAI MYLION MEDICAL CONSULTING CO., LTD., |
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研究负责人所在单位: |
上海长海医院 |
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Affiliation of the Leader: |
Shanghai Changhai 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: |
CHEC2022-188 |
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: |
上海长海医院伦理委员会 |
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Name of the ethic committee: |
Shanghai Changhai Hospital Ethics Committee |
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伦理委员会批准日期: Date of approved by ethic committee: |
2022-09-30 00:00:00 |
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伦理委员会联系人: |
计一平 |
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Contact Name of the ethic committee: |
Yiping Ji |
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伦理委员会联系地址: |
上海市杨浦区长海路168号 |
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Contact Address of the ethic committee: |
168 Changhai Road, Yangpu District, Shanghai, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 21 31162338 |
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: |
上海长海医院 |
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Primary sponsor: |
Shanghai Changhai Hospital |
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研究实施负责(组长)单位地址: |
上海市杨浦区长海路168号 |
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Primary sponsor's address: |
168 Changhai Road, Yangpu District, Shanghai, 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: |
上海长海医院消化内科 |
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Source(s) of funding: |
Department of Gastroenterology, Shanghai Changhai Hospital |
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Target disease: |
functional dyspepsia |
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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: |
以安慰剂为对照,用药4周,评估得必泰改善FD患者主要症状的有效性和安全性,为该药用于FD的临床治疗提供依据 |
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Objectives of Study: |
To evaluate the efficacy and safety of Debitai in improving the main symptoms of FD patients with placebo for 4 weeks, so as to provide a basis for the clinical treatment of FD |
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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 18~65 周岁,男女不限,门诊患者; |
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Inclusion criteria |
(1) Outpatients aged 18-65, male and female; |
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排除标准: |
(1)患有甲状腺疾病、系统性硬化症、系统性红斑狼疮、慢性胆囊炎、胆囊结石及其他严重肝胆胰疾病;或考虑有肠梗阻可能性; |
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Exclusion criteria: |
(1) Suffering from thyroid disease, systemic sclerosis, systemic lupus erythematosus, chronic cholecystitis, gallstones and other serious hepatobiliary and pancreatic diseases; Or consider the possibility of intestinal obstruction; |
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研究实施时间: Study execute time: |
从 From 2022-08-01 00:00:00至 To 2024-08-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2023-03-01 00:00:00 至 To 2023-09-01 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): |
随机分配编码由统计学专业人员用 SAS 统计软件在计算机上模拟产生,将随机编号分段发至各试验中心,并配备相应的治疗药盒,研究者按受试者就诊先后顺序,选用对应序号的药盒进行治疗 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
The randomly assigned codes were simulated by statistical professionals using SAS statistical software on the computer, and the random numbers were sent to each experimental center in sections, and corresponding treatment boxes were equipped. The researchers selected the corresponding serial numbers of the drug boxes f |
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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: |
采用两级盲法设计,第一级为各病例号所对应的组别(如 A组、B组),第二级为各组所对应的处理(试验组和对照组)。随机编码表由统计单位建立,两级盲底分别单独密封,各一式叁份,分别存放于各研究中心、组长单位及申办者处。 |
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Blinding: |
A two-stage blind design was adopted. The first stage was the group corresponding to each case number (such as group A and group B), and the second stage was the treatment corresponding to each group (experimental group and control group). The random coding table is established by the statistical unit, and the two levels of blind bottom are separately sealed, each in triplicate, and stored in each research center, the group leader unit and the sponsor respectively. |
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是否共享原始数据: IPD sharing |
No |
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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): |
NA |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
NA |
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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: |
NA |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
NA |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |