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注册号: Registration number: |
ChiCTR2300071812 |
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最近更新日期: Date of Last Refreshed on: |
2023-07-03 15:37:55 |
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注册时间: Date of Registration: |
2023-05-25 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: |
研究者撤销 伏诺拉生-阿莫西林二联治疗用于幽门螺杆菌感染根除对肠道微生态的影响 |
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Public title: |
Canceled by the investigator Effect of vonoprazan-amoxicillin dual therapy on gut microbiota |
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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: |
伏诺拉生-阿莫西林二联治疗用于幽门螺杆菌感染根除对肠道微生态的影响 |
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Scientific title: |
Effect of vonoprazan-amoxicillin dual therapy on gut microbiota |
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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: |
徐婷婷 |
研究负责人: |
徐婷婷 |
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Applicant: |
Tingting Xu |
Study leader: |
Tingting Xu |
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申请注册联系人电话: Applicant telephone: |
+86 130 6986 3801 |
研究负责人电话:
Study leader's |
+86 130 6986 3801 |
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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: |
452064807@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
452064807@qq.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: |
海南省文昌市文城镇文清大道289号 |
研究负责人通讯地址: |
海南省文昌市文城镇文清大道289号 |
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Applicant address: |
289 Wenqing Avenue, Wencheng Town, Wenchang, Hainan |
Study leader's address: |
289 Wenqing Avenue, Wencheng Town, Wenchang, Hainan |
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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: |
文昌市人民医院/同济文昌医院 |
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Applicant's institution: |
Wenchang People's Hospital |
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研究负责人所在单位: |
文昌市人民医院/同济文昌医院 |
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Affiliation of the Leader: |
Wenchang People's 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: |
(2023)伦审(01-01)号 |
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: |
文昌市人民医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Wenchang People's Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-05-06 00:00:00 | ||
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伦理委员会联系人: |
符国展 |
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Contact Name of the ethic committee: |
Guozhan Fu |
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伦理委员会联系地址: |
海南省文昌市文城镇文清大道289号 |
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Contact Address of the ethic committee: |
289 Wenqing Avenue, Wencheng Town, Wenchang, Hainan |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 130 7899 4935 |
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: |
文昌市人民医院/同济文昌医院 |
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Primary sponsor: |
Wenchang People's Hospital |
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研究实施负责(组长)单位地址: |
海南省文昌市文城镇文清大道289号 |
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Primary sponsor's address: |
289 Wenqing Avenue, Wencheng Town, Wenchang, Hainan |
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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: |
自筹 |
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Source(s) of funding: |
self-funding |
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研究疾病: |
幽门螺杆菌 |
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Target disease: |
Helicobacter pylori |
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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: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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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: |
旨在评估伏诺拉生-阿莫西林二联治疗的根除疗效和安全性,与此同时,还将比较不同治疗时间(10天vs 14天)的疗效和安全性,并探究其对肠道菌群的影响。 |
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Objectives of Study: |
To evaluate the eradication efficacy and safety of 10-day and 14-day vonoprazan-amoxicillin dual therapy and explore the effect of vonoprazan-amoxicillin dual therapy on gut microbiota. |
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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: |
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Inclusion criteria |
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排除标准: |
1. 曾行H. pylori根除治疗; 2. 在筛选前 12个月内有酒精滥用、非法药物使用或药物成瘾史,或每周饮用>21个单位的酒精(6300 mL啤酒,525 mL烈酒,或2100mL葡萄酒); 3. 过去3月内有抗生素、益生菌、PPI、抗病毒/真菌药物,NSAIDs、黏膜保护剂、免疫抑制剂或激素等服用史; 4. 近4周服用过泻药或出现急性胃肠炎; 5. 孕期及哺乳期; 6. 过度肥胖; 7. 存在青霉素或方案相关药物过敏史; 8. 正在参加另一项临床研究者; 9. 研究者认为不适合纳入者。 |
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Exclusion criteria: |
1. With a history of H. pylori eradication; 2. Alcohol abuse, illicit drug use or drug addiction, or consumption of >21 units of alcohol per week (6300 mL beer, 525 mL spirits, or 2100mL wine) in the 12 months prior to screening; 3. Taking antibiotics, probiotics, PPI, antiviral/fungal drugs, NSAIDs, mucosal protectants, immunosuppressants or hormones in the past 3 months; 4.Taking laxatives or having acute gastroenteritis in the past 4 weeks; 5. Pregnancy and lactation; 6. Excessive obesity; 7. Allergy to penicillin or other drug in this study; 8. Currently participating in another clinical study; 9. Patients assessed as unsuitable by investigators. |
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研究实施时间: Study execute time: |
从 From 2023-06-01 00:00:00至 To 2024-06-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-06-01 00:00:00 至 To 2024-04-30 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): |
随机数列表 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Random number list |
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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: |
无 |
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Blinding: |
None |
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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): |
以文章发表形式公开 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
In the form of published article |
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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: |
患者的数据将保存于SPSS数据库 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
SPSS database |
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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 |