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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: |
ChiCTR2200067204 |
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最近更新日期: Date of Last Refreshed on: |
2022-12-29 15:02:48 |
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注册时间: Date of Registration: |
2022-12-29 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: |
胆宁片治疗胆囊息肉样病变的临床研究 |
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Public title: |
A study of Danning tablet in patients with polypoid lesions of gallbladder |
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注册题目简写: |
胆囊息肉样病变(PLG)临床研究 |
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English Acronym: |
PLG001 |
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研究课题的正式科学名称: |
生活方式干预下,联合或不联合胆宁片治疗胆囊息肉样病变的随机、开放、对照、多中心临床试验 |
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Scientific title: |
Effects of Danning tablet under lifestyle intervention in patients with polypoid lesions of gallbladder :A Randomized, Open-labelled, Multicenter, Controlled Trial |
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研究课题代号(代码): Study subject ID: |
CCPE202201 |
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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: |
杨田 |
研究负责人: |
沈锋/杨田 |
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Applicant: |
Tian Yang |
Study leader: |
Feng Shen/Tian Yang |
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申请注册联系人电话: Applicant telephone: |
18917015805 |
研究负责人电话:
Study leader's |
13901651428 |
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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: |
yangtianehbh@smmu.edu.cn |
研究负责人电子邮件: Study leader's E-mail: |
shenfengehbh@sina.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: |
上海市杨浦区长海路225号 |
研究负责人通讯地址: |
上海市杨浦区长海路225号 |
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Applicant address: |
No. 225, Changhai Road, Yangpu District, Shanghai City |
Study leader's address: |
No. 225, Changhai Road, Yangpu District, Shanghai City |
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申请注册联系人邮政编码: Applicant postcode: |
200433 |
研究负责人邮政编码: Study leader's postcode: |
200433 |
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申请人所在单位: |
海军军医大学第三附属医院(上海东方肝胆外科医院) |
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Applicant's institution: |
The Third Affiliated Hospital of Naval Medical University (East hepatobiliary Hospital) |
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研究负责人所在单位: |
海军军医大学第三附属医院(上海东方肝胆外科医院) |
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Affiliation of the Leader: |
The Third Affiliated Hospital of Naval Medical University (East hepatobiliary 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: |
EHBHKY2022-H038-P001 |
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: |
海军军医大学第三附属医院医学伦理委员会 |
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Name of the ethic committee: |
Ethic Committee of the Third Affiliated Hospital of Naval Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2022-11-24 00:00:00 | ||
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伦理委员会联系人: |
邰小云 |
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Contact Name of the ethic committee: |
Xiaoyun Tai |
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伦理委员会联系地址: |
上海市杨浦区长海路225号 |
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Contact Address of the ethic committee: |
No. 225, Changhai Road, Yangpu District, Shanghai City |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 15221390719 |
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: |
海军军医大学第三附属医院(上海东方肝胆外科医院) |
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Primary sponsor: |
The Third Affiliated Hospital of Naval Medical University (East hepatobiliary 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225号 |
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Primary sponsor's address: |
No. 225, Changhai Road, Yangpu District, Shanghai City |
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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: |
海军军医大学第三附属医院(上海东方肝胆外科医院) |
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Source(s) of funding: |
The Third Affiliated Hospital of Naval Medical University (East hepatobiliary Hospital) |
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研究疾病: |
胆囊息肉样病变 |
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Target disease: |
polypoid lesions of gallbladder |
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研究疾病代码: |
K82.802;DC10.3 |
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Target disease code: |
K82.802;DC10.3 |
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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: |
主要目的:评价在生活方式干预基础上,口服胆宁片使胆囊息肉缩小的效果。 次要目的: 1) 评价口服胆宁片缓解胆囊息肉临床症状的效果(可能有症状); 2) 评价胆宁片治疗胆囊息肉的安全性。 |
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Objectives of Study: |
Primary objective: To evaluate the effect of Danning tablet on shrinkage of gallbladder polyps under lifestyle intervention. Secondary objective: 1) To evaluate the effect of Danning tablet on alleviation of clinical symptoms of gallbladder polyps (there may be symptoms). 2) To evaluate the safety of Danning tablet in treatment of gallbladder polyps. |
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药物成份或治疗方案详述: |
试验组在生活方式干预的基础上服用胆宁片(5片/次,3次/天),从入组开始连续服用12周;对照组将在入组后采用单纯的生活方式干预,两组患者的随访期均为24周。 |
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Description for medicine or protocol of treatment in detail: |
Under lifestyle intervention, in test group, Danning Tablets will be taken orally from baseline to weeks 12±1 (3 times each day, 5 tablets each time). In controlled group, only lifestyle intervention will be adopted. The length of the follow-up cycle is 24 weeks. |
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纳入标准: |
适合入组本研究的受试者必须符合以下所有标准: |
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Inclusion criteria |
Subjects suitable for enrollment in this study must meet all of the following criteria: |
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排除标准: |
凡符合以下任何一项标准的受试者不得入选本研究: |
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Exclusion criteria: |
Subjects who meet any of the following criteria will not be eligible for inclusion in this study: |
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研究实施时间: Study execute time: |
从 From 2022-10-17 00:00:00至 To 2024-11-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-01-01 00:00:00 至 To 2024-05-31 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: |
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): |
采用区组随机,利用SAS统计软件,选取合适段长,按1:1比例分为试验组或对照组。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Adopt blocked randomization method, use SAS to generate random table. The subjects will be randomly allocated to the test group or controlled group in ratio of 1:1. |
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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: |
开放标签,不设置盲法。 |
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Blinding: |
Open labelled, blinding not involved. |
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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 |
否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): |
不共享 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
No |
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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: |
采用电子采集和管理系统(EDC)中的电子病例记录表(eCRF)记录研究相关数据,并在研究过程中对记录在EDC的数据进行核查,核查过程中的疑问,由EDC自动生成的疑问及人工核查发出的疑问两种形式产生,由研究者进行答疑,直至数据清理干净。最终疑问均由研究者确认签字。数据管理部门保存疑问表电子版。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Use electronic case report form (eCRF) in the electronic data capture (EDC) system to record relevant data of the study. Data reported in EDC is monitored regularly during the study cycle. The queries are generated automatically by EDC or manually during data management process. The investigator should answer the queries until all the queries are cleared out. The final query table should be confirmed and signed by the investigator. The data management department should keep the electronic version of the query table. |
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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 |