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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: |
ChiCTR2400090984 |
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最近更新日期: Date of Last Refreshed on: |
2024-10-17 09:51:08 |
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注册时间: Date of Registration: |
2024-10-17 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
利拉鲁肽注射液(利鲁平)治疗超重或肥胖患者的多中心、前瞻性、观察性研究 |
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Public title: |
A Multicenter, Prospective, Observational Study of Liraglutide Injection (Rilupine) in the Treatment of Overweight or Obese Patients |
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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: |
利拉鲁肽注射液(利鲁平)治疗超重或肥胖患者的多中心、前瞻性、观察性研究 |
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Scientific title: |
A Multicenter, Prospective, Observational Study of Liraglutide Injection (Rilupine) in the Treatment of Overweight or Obese Patients |
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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: |
钱晓芬 |
研究负责人: |
胡玲 |
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Applicant: |
Qian xiaofen |
Study leader: |
Hu Ling |
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申请注册联系人电话: Applicant telephone: |
+86 178 5768 5233 |
研究负责人电话:
Study leader's |
+86 139 7007 5119 |
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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: |
qianxiaofen@eastchinapharm.com |
研究负责人电子邮件: Study leader's E-mail: |
hul@medmail.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莫干路858号 |
研究负责人通讯地址: |
南昌市东湖区象山北路128号 |
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Applicant address: |
No. 858 Mogan Road, Gongshu District, Hangzhou City, Zhejiang Province |
Study leader's address: |
128 Xiangshan North Road, Donghu District, Nanchang City |
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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: |
杭州中美华东制药有限公司 |
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Applicant's institution: |
Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd |
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研究负责人所在单位: |
南昌市第一医院 |
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Affiliation of the Leader: |
Nanchang First 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: |
审2024(003) |
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: |
南昌市第一医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Nanchang First Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-04-28 00:00:00 | ||
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伦理委员会联系人: |
琴丽英 |
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Contact Name of the ethic committee: |
QinLiying |
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伦理委员会联系地址: |
江西省南昌市东湖区象山北路128号 |
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Contact Address of the ethic committee: |
128 Xiangshan North Road, Donghu District, Nanchang City |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 791 8677 1017 |
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: |
南昌市第一医院 |
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Primary sponsor: |
Nanchang First Hospital |
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研究实施负责(组长)单位地址: |
江西省南昌市东湖区象山北路128号 |
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Primary sponsor's address: |
128 Xiangshan North Road, Donghu District, Nanchang 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: |
杭州中美华东制药有限公司 |
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Source(s) of funding: |
Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd |
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研究疾病: |
超重或肥胖 |
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Target disease: |
overweight or obese |
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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: |
观察性研究 |
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Study type: |
Observational 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: |
连续入组 |
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Study design: |
Sequential |
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研究目的: |
主要目的: 评价利拉鲁肽注射液在实际临床中治疗超重/肥胖患者体重控制的有效性和安全性。 次要目的: (1) 评价利拉鲁肽注射液在实际临床中对超重/肥胖伴随 2 型糖尿病患者血糖控制的有效性和安性; (2) 评估利拉鲁肽注射液临床实际治疗的用法用量、疗程、合并用药情况等; (3) 评价利拉鲁肽注射液对超重/肥胖合并心血管疾病或肾病患者心肾的额外获益。 |
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Objectives of Study: |
Primary Objectives: To evaluate the efficacy and safety of liraglutide injection in the treatment of weight control in overweight/obese patients in practice. Secondary Purpose: (1) To evaluate the effectiveness and safety of liraglutide injection in clinical practice for glycemic control in patients with overweight/obesity with type 2 diabetes mellitus; (2) To evaluate the dosage, course of treatment, and concomitant medication of liraglutide injection; (3) To evaluate the additional benefit of liraglutide injection on the heart and kidney in patients with overweight/obesity complicated with cardiovascular disease or kidney disease. |
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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 周岁,性别不限; (2)筛选时受试者 24.0 kg/m2≤体重指数(BMI)<28.0 kg/m2 [体重指数 BMI=体重(kg)/身高 2(m2)],并伴有至少一种体重相关合并症,或体重指数(BMI≥28.0kg/m2,无论是否有合并症;且体重保持稳定(3 个月内自述体重变化小于 5%); (3) 超重/肥胖伴随高血压、糖尿病、血脂异常等合并症者需符合相关疾病诊断标准(可参考《国家基层高血压防治管理指南(2020 版)》、《中国 2 型糖尿病防治指南(2020 年版)》及《中国血脂管理指南(2023 年)》等指南要求),其中超重/肥胖伴随糖尿病者需有入组前 1 个月内糖化血红蛋白(HbA1c)检查结果; (4) 首次接受利拉鲁肽注射液(利鲁平)治疗; (5) 自愿参加研究并签署知情同意书。 |
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Inclusion criteria |
(1) Age≥ 18 years old, gender is not limited; (2) Subject 24.0 kg/m2≤ body mass index (BMI)<28.0 kg/m2 [body mass index BMI=weight (kg)/height 2(m2)] at screening, with at least one weight-related comorbidity, or body mass index (BMI≥28.0kg/m2, with or without comorbidities; and stable body weight (less than 5% self-reported weight change within 3 months); (3) Patients with overweight/obesity with comorbidities such as hypertension, diabetes mellitus, and dyslipidemia must meet the relevant disease diagnostic criteria (please refer to the guidelines for the prevention and management of primary hypertension at the national level (2020 edition), the guidelines for the prevention and treatment of type 2 diabetes in China (2020 edition) and the guidelines for the management of blood lipids in China (2023), among which overweight/obesity with diabetes mellitus must have glycosylated hemoglobin (HbA1c) test results within 1 month before enrollment; (4) First treatment with liraglutide injection (rilupine); (5) Voluntarily participate in the study and sign the informed consent form. |
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排除标准: |
(1) 甲状腺髓样癌(MTC)或多发性内分泌腺瘤病 2 型(MEN2)的个人史或家族史; (2) 对利拉鲁肽或者本品的任何辅料成分有严重过敏史; (3) 目前或过去 1 个月内参加任何其他临床试验; (4) 经研究者判断不适合参加本次研究。 |
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Exclusion criteria: |
(1) Personal or family history of medullary thyroid cancer (MTC) or multiple endocrine neoplasia type 2 (MEN2); (2) Have a history of severe allergy to liraglutide or any excipient component of this product; (3) Participation in any other clinical trial currently or within the past 1 month; (4) Not suitable to participate in this study as judged by the investigator. |
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研究实施时间: Study execute time: |
从 From 2023-12-31 00:00:00至 To 2026-06-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-07-19 00:00:00 至 To 2025-12-31 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: |
正在进行 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): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
N/A |
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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: |
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Blinding: |
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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): |
发表文章后 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
After publishing the paper |
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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: |
CRF |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF |
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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 |