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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: |
ChiCTR2500103593 |
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最近更新日期: Date of Last Refreshed on: |
2025-05-30 18:05:43 |
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注册时间: Date of Registration: |
2025-05-30 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: |
富氢水辅助治疗肥胖的探索性临床研究 |
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Public title: |
Hydrogen-Rich Water as an Adjuvant Therapy for Obesity:one exploratory clinical study |
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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: |
富氢水辅助治疗肥胖的探索性临床研究 |
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Scientific title: |
Hydrogen-Rich Water as an Adjuvant Therapy for Obesity:one exploratory clinical study |
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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: |
张含兵 |
研究负责人: |
张含兵 |
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Applicant: |
Zhang Hanbing |
Study leader: |
Zhang Hanbing |
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申请注册联系人电话: Applicant telephone: |
+86 150 6417 3082 |
研究负责人电话:
Study leader's |
+86 150 6417 3082 |
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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: |
zhanghanbing271413@126.com |
研究负责人电子邮件: Study leader's E-mail: |
zhanghanbing271413@126.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: |
山东省泰安市泰山区龙潭路29号 |
研究负责人通讯地址: |
山东省泰安市泰山区龙潭路29号 |
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Applicant address: |
No. 29 Longtan Road, Taishan District, Tai'an City, Shandong Province, China |
Study leader's address: |
No. 29 Longtan Road, Taishan District, Tai'an City, Shandong Province, China |
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申请注册联系人邮政编码: Applicant postcode: |
271000 |
研究负责人邮政编码: Study leader's postcode: |
271000 |
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申请人所在单位: |
泰安市中心医院 |
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Applicant's institution: |
Tai'an Central Hospital |
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研究负责人所在单位: |
泰安市中心医院 |
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Affiliation of the Leader: |
Tai'an Central 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: |
2025-06-27 |
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: |
泰安市中心医院医学伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Tai'an Central Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-05-20 00:00:00 | ||
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伦理委员会联系人: |
王兴玲 |
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Contact Name of the ethic committee: |
Wang Xingling |
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伦理委员会联系地址: |
山东省泰安市泰山区龙潭路29号 |
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Contact Address of the ethic committee: |
No. 29 Longtan Road, Taishan District, Tai'an City, Shandong Province, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 538 629 8222 |
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: |
泰安市中心医院 |
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Primary sponsor: |
Tai'an Central Hospital |
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研究实施负责(组长)单位地址: |
山东省泰安市泰山区龙潭路29号 |
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Primary sponsor's address: |
No. 29 Longtan Road, Taishan District, Tai'an City, Shandong Province, 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: |
单位自筹 |
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Source(s) of funding: |
Self-raised institutional funds |
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研究疾病: |
肥胖症 |
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Target disease: |
Obesity |
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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: |
I期临床试验 | ||||||||||||||||||||||
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Study phase: |
1 |
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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: |
探讨氢分子对肥胖患者体重、腰围、体脂率及代谢指标(如血糖、血脂、胰岛素敏感性)的影响,同时研究氢分子治疗肥胖的可能机制,包括氧化应激、炎症反应和肠道菌群的变化。 |
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Objectives of Study: |
To investigate the effects of molecular hydrogen on body weight, waist circumference, body fat percentage, and metabolic parameters (e.g., blood glucose, lipid profile, and insulin sensitivity) in obese patients. Additionally, this study aims to explore the potential mechanisms underlying hydrogen therapy for obesity, including oxidative stress, inflammatory responses, and alterations in 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: |
参考 2024年国家卫生健康委员会医政司制定的《肥胖症诊疗指南(2024年版)》:BMI达到 24 kg/m2 且低于 28 kg/m2 为超重,达到或超过 28 kg/m2 为肥胖。 纳入标准:符合超重或肥胖症诊断标准;年龄在 18~65 岁之间;没有兼用其他可能会影响体质量的药物;自愿参加本课题并签署 《知情同意书》。 |
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Inclusion criteria |
Reference: Based on the 2021 Expert Consensus on Body Weight Management Procedures for Overweight/Obese Populations issued by the Health Management Branch of the Chinese Medical Association: Overweight: 24 kg/m^2 <= BMI < 28 kg/m^2 Obesity: BMI >= 28 kg/m^2 Central obesity (adults): Waist circumference ≥ 90 cm (male) or ≥ 85 cm (female). Inclusion Criteria: Meeting the diagnostic criteria for overweight or obesity; Aged 16–65 years; No concurrent use of medications that may affect body weight; Voluntary participation with signed informed consent. |
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排除标准: |
排除标准:继发性肥胖者,如下丘脑病变以及内分泌系统疾病如皮质醇 增多症、甲状腺功能低下、胰岛素细胞瘤等引起的肥胖,或 因药物引起的肥胖 ;妊娠期及哺乳期或未来 6 个月内准备怀 孕的妇女 ;合并有严重心、肝、肾等重要脏器的原发性疾病者;合并凝血系统障碍、感染性疾病、恶性肿瘤、肝硬化等 严重疾病者 ;治疗前 3 个月内接受过减肥药物或其他任何减 肥治疗,或 3 个月内体质量下降>5% ;不能配合治疗与随访者。 |
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Exclusion criteria: |
Exclusion Criteria:Secondary obesity caused by:Hypothalamic disorders;Endocrine diseases (e.g., hypercortisolism, hypothyroidism, insulinoma);Medication-induced weight gain;Pregnancy, lactation, or women planning pregnancy within 6 months;Severe primary diseases of major organs (heart, liver, kidney);Coexisting severe conditions:Coagulation disorders;Infectious diseases;Malignancies;Liver cirrhosis;Any weight-loss medication or treatment within 3 months prior to enrollment, or >5% body weight reduction during this period;Inability to comply with treatment and follow-up protocols |
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研究实施时间: Study execute time: |
从 From 2025-06-01 00:00:00至 To 2026-09-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-06-01 00:00:00 至 To 2026-06-30 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): |
随机和隐蔽分组的方法: 该试验设计预计纳入60例患者,按照就诊时间顺序进行编为1-60号,将写有1-60数字的纸条装入密闭信封,由我院医务部工作人员使用抽签法确定分组,具体为:第1个抽到的信封,内有的数字号代表的患者进入A管道组,第2个抽到的信封,内有的数字号代表的患者进入B管道组。该医务部工作人员不参与临床试验运行,严格保存分配表。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
This trial is designed to enroll 60 patients, who will be sequentially numbered from 1 to 60 based on their visit order. Slips of paper labeled with numbers 1 to 60 will be placed in sealed envelopes. A staff member from the hospital’s medical administration department will determine group allocation by drawing lots. |
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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: |
双盲 |
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Blinding: |
Double blinding |
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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 |
是Yes |
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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): |
自实验开始,原始数据在ResMan临床试验公共管理平台共享。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
From the initiation of the trial, all raw data will be shared on the ResMan clinical trial public management platform |
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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: |
每位受试者均有一份纸质版研究者病历,详细记录患者基本信息及实验过程;试验结束后,纸质版病历扫描并上传ResMan临床试验公共管理平台。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Each participant has a paper-based investigator case report form (CRF) that comprehensively documents baseline information and the trial process. Upon trial completion, these paper records are scanned and uploaded to the ResMan Clinical Trial Public Management Platform. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |