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注册号: Registration number: |
ChiCTR2600119644 |
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最近更新日期: Date of Last Refreshed on: |
2026-03-02 10:05:10 |
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注册时间: Date of Registration: |
2026-03-02 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: |
一项多中心、前瞻性、随机对照研究探索不同给药时间间隔的肠菌胶囊治疗肝性脑病的有效性和安全性 |
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Public title: |
A Multicenter, Prospective, Randomized Controlled Study to Explore the Efficacy and Safety of Encapsulated Fecal Microbiota Transplantation with Different Dosing Intervals in the Treatment of Hepatic Encephalopathy |
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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: |
一项全国多中心、前瞻性、随机对照研究探索不同给药时间间隔的肠菌胶囊治疗肝性脑病的有效性和安全性 |
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Scientific title: |
A National Multicenter, Prospective, Randomized Controlled Study Exploring the Efficacy and Safety of Fecal Microbiota Capsules With Different Dosing Intervals for the Treatment of Hepatic Encephalopathy |
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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: |
邹鹏飞 |
研究负责人: |
高海女 |
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Applicant: |
Pengfei Zou |
Study leader: |
Hainv Gao |
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申请注册联系人电话: Applicant telephone: |
+86 138 5811 5506 |
研究负责人电话:
Study leader's |
+86 139 5716 3067 |
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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: |
474329859@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
gaohainv@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: |
浙江省杭州市拱墅区东新路848号树兰(杭州)医院感染科 |
研究负责人通讯地址: |
浙江省杭州市拱墅区东新路848号树兰(杭州)医院感染科 |
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Applicant address: |
No.848 Dongxin Road, Gongshu District, Hangzhou, Zhejiang, China |
Study leader's address: |
No.848 Dongxin Road, Gongshu District, Hangzhou, Zhejiang, 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: |
树兰(杭州)医院 |
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Applicant's institution: |
Shulan (Hangzhou) Hospital |
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研究负责人所在单位: |
树兰(杭州)医院 |
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Affiliation of the Leader: |
Shulan (Hangzhou) 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: |
KY2025175 |
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: |
树兰(杭州)医院伦理委员会 |
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Name of the ethic committee: |
Shulan (Hangzhou) Hospital Ethics Committee |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-12-24 00:00:00 | ||
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伦理委员会联系人: |
管文花 |
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Contact Name of the ethic committee: |
Guan Wenhua |
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伦理委员会联系地址: |
浙江省杭州市拱墅区东新路848号 |
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Contact Address of the ethic committee: |
No.848 Dongxin Road, Gongshu District, Hangzhou, Zhejiang, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 138 6718 0055 |
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: |
树兰(杭州)医院 |
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Primary sponsor: |
hulan (Hangzhou) Hospital |
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研究实施负责(组长)单位地址: |
浙江省杭州市拱墅区东新路848号 |
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Primary sponsor's address: |
No.848 Dongxin Road, Gongshu District, Hangzhou, Zhejiang, 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: |
国家重点研发计划 (2021YFA1301104) |
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Source(s) of funding: |
The National Key Research and Development Program of China (2021YFA1301104) |
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研究疾病: |
肝性脑病 |
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Target disease: |
Hepatic encephalopathy |
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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: |
1、评估不同时间间隔的肠菌胶囊(cFMT)治疗肝性脑病的有效性、安全性; 2、探索肠菌胶囊治疗肝性脑病的合理治疗方案。 |
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Objectives of Study: |
To evaluate the effectiveness and safety of Encapsulated Fecal Microbiota Transplantation (cFMT) with Different Dosing Intervals in the Treatment of Hepatic Encephalopathy, and to explore a reasonable therapeutic scheme of cFMT for hepatic encephalopathy. |
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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: |
1.1个月内预期进行肝移植的患者; 2.3个月内存在已知的肝性脑病诱因(包括胃肠道出血)的患者; 3.存在慢性肾功能不全(肌酐水平>2.0mg/dl)、呼吸功能不全、贫血(Hb<8g/dl)、电解质异常(血清钠<125umol/L;血清钙>10mg/dl[2.5umol/L];或血清钾<2.5 mmol/l)并发感染,或活动性、自发性细菌性腹膜炎; 4.在近12周内有大量饮酒; 5.在近4周内使用过影响心理测量肝性脑病评分(PHES)的药物,如抗抑郁药和镇静催眠; 6.对治疗前的抗生素过敏的患者; 7.cFMT 时感染(根据需要通过血培养阳性、尿液分析、穿刺术进行诊断); 8.患有慢性内源性胃肠道疾病的患者,如炎症性肠病(溃疡性结肠炎、克罗恩病或显微镜下结肠炎)、肠易激综合征; 9.患有神经系统疾病,如中风、癫痫、痴呆和帕金森病; 10.怀孕或哺乳的患者(将使用尿妊娠试验进行检查); 11.未控制的肝脏恶性肿瘤或其他部位的恶性肿瘤; 12.存在吞咽困难或肠道梗阻,无法口服胶囊的患者; 13.其他研究者认为不适合纳入本试验者; 14.无法提供知情同意书的患者 |
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Exclusion criteria: |
1. Patients expected to undergo liver transplantation within 1 month; 2. Patients with known causes of hepatic encephalopathy (including gastrointestinal bleeding) within 3 months; 3. There are chronic renal insufficiency (creatinine level > 2.0 mg/dl), respiratory insufficiency, anemia (HB < 8 g/dl), electrolyte abnormalities (serum sodium < 125 umol/L; serum calcium > 10 mg/dl [2.5 umol/L]; or serum potassium < 2.5 mmol/L) complicated with infection, or active and spontaneous bacterial peritonitis; 4. Heavy drinking in recent 12 weeks; 5. Have used drugs that affect the psychometric score of hepatic encephalopathy (PHEs), such as antidepressants and sedative hypnosis, in recent 4 weeks; 6. Patients who are allergic to antibiotics before treatment; 7. Infection during cFMT (diagnosis by positive blood culture, urinalysis and puncture); 8. Patients with chronic endogenous gastrointestinal diseases, such as inflammatory bowel disease (ulcerative colitis, Crohn's disease or microscopic colitis), irritable bowel syndrome; 9. Suffering from neurological diseases, such as stroke, epilepsy, dementia and Parkinson's disease; 10. Pregnant or lactating patients (urine pregnancy test will be used for examination); 11.Uncontrolled hepatic or other systemic malignancies; 12.Patients with dysphagia or intestinal obstruction precluding oral capsule intake; 13.Other researchers think it is not suitable to be included in this experiment; 14. Patients who cannot provide informed consent. |
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研究实施时间: Study execute time: |
从 From 2025-12-24 00:00:00至 To 2027-05-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-03-04 00:00:00 至 To 2026-11-30 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): |
符合所有入选标准而不符合任一排除标准的受试者接受随机分配。产生的随机号码由独立于项目的统计师编成,使用SAS9.4按照1:1的比例产生随机序列,将受试者按照就诊的先后顺序随机分入两组。该随机号唯一对应该受试者,不能被重复使用。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Subjects who met all enrollment criteria but did not meet any of the exclusion criteria were randomized. The generated random numbers were compiled by statisticians independent of project. SAS9.4 was used to generate a random sequence in a 1: 1 ratio, and the subjects were randomly divided into two grou |
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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): |
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 share. |
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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: |
数据采集和管理通过病例记录表(Case Record Form, CRF)以及电子电子病历系统完成。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Data collection and management are completed by Case Record Form, CRF) and electronic medical record system. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |