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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: |
ChiCTR-IPR-15006894 |
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最近更新日期: Date of Last Refreshed on: |
2016-07-27 21:24:46 |
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注册时间: Date of Registration: |
2015-08-07 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: |
在中国2型糖尿病患者中使用甘精胰岛素的滴定目标:三种不同空腹血糖目标评价 |
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Public title: |
Titration target for Chinese type 2 diabetes mellitus patients using insulin glargine to achieve glycaemic goals: an assessment of three different fasting plasma glucose targets |
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注册题目简写: |
BEYOND III/FPG GOAL |
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English Acronym: |
BEYOND III/FPG GOAL |
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研究课题的正式科学名称: |
在中国2型糖尿病患者中使用甘精胰岛素的滴定目标:三种不同空腹血糖目标评价-BEYOND III/FPG GOAL研究 |
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Scientific title: |
Titration target for Chinese type 2 diabetes mellitus patients using insulin glargine to achieve glycaemic goals: an assessment of three different fasting plasma glucose targets - BEYOND III/FPG GOAL Study |
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研究课题代号(代码): Study subject ID: |
LANTUL07190 |
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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: |
刘青 |
研究负责人: |
刘微 |
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Applicant: |
LIU Qing |
Study leader: |
Wei LIU |
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申请注册联系人电话: Applicant telephone: |
+86 21 22266623 |
研究负责人电话:
Study leader's |
+86 10 65634707 |
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申请注册联系人传真 : Applicant Fax: |
+86 21 60123538 |
研究负责人传真: Study leader's fax: |
+86 10 85215223 |
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申请注册联系人电子邮件: Applicant E-mail: |
qing1.liu@sanofi.com |
研究负责人电子邮件: Study leader's E-mail: |
wei12.liu@sanofi.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: |
上海市静安区延安中路1228号静安嘉里中心办公楼3座19楼 |
研究负责人通讯地址: |
北京市朝阳区建国路108号海航实业大厦3层 |
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Applicant address: |
19F Tower III, Kerry Center, 1228 Middle Yan'an Road, Jing'an District, Shanghai |
Study leader's address: |
3F, Haihang Building, 108 Jianguo Road, Chaoyang District, Beijing |
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申请注册联系人邮政编码: Applicant postcode: |
200040 |
研究负责人邮政编码: Study leader's postcode: |
100022 |
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申请人所在单位: |
赛诺菲(中国)投资有限公司上海分公司 |
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Applicant's institution: |
SANOFI (CHINA) INVESTMENT CO., LTD. SHANGHAI BRANCH |
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研究负责人所在单位: |
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Affiliation of the Leader: |
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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: |
2015-69 |
伦理委员会批件附件: Approved file of Ethical Committee: |
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批准本研究的伦理委员会名称: |
中日友好医院药品临床研究伦理委员会 |
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Name of the ethic committee: |
Clinical Trial Ethic Committee of China-Japan Friendship Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2015-08-06 00:00:00 | ||
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伦理委员会联系人: |
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Contact Name of the ethic committee: |
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伦理委员会联系地址: |
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Contact Address of the ethic committee: |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
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: |
中日友好医院 |
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Primary sponsor: |
China-Japan Friendship Hospital |
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研究实施负责(组长)单位地址: |
北京市朝阳区樱花东路2号 |
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Primary sponsor's address: |
2 Yinghua East Road, Chaoyang District, Beijing |
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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: |
赛诺菲(北京)制药有限公司 |
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Source(s) of funding: |
Sanofi (Beijing) Pharmaceuticals Co., Ltd |
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研究疾病: |
2型糖尿病 |
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Target disease: |
Type 2 diabetes mellitus |
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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: |
IV期临床试验 | ||||||||||||||||||||||
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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: |
1. 为使用甘精胰岛素治疗的中国2型糖尿病患者确定一个最佳的FPG目标,以获得最高的HbA1c<7%达标率 2. HbA1c ≤ 6.5% 的达标率 3. FPG目标达标患者中HbA1c < 7%的达标率 4. HbA1c < 7%且无低血糖的患者比例 5. FPG目标达标且无低血糖的患者比例 6. FPG目标和PPG目标(早餐后2小时血糖 < 10 mmol/L)达标的患者比例 7. 满足HbA1c < 7%,FPG > 7 mmol/L、> 6.1 且≤ 7 mmol/L、> 5.6 且≤ 6.1 mmol/L、 >5.0 且≤ 5.6 mmol/L 及 ≤ 5 mmol/L 且无低血糖的患者比例 8. HbA1c 较基线的下降 9. FPG 和PPG 的下降 10. 研究结束时各组的最终胰岛素剂量 11. 各治疗组从研究开始至结束的体重变化 12. 低血糖的发生率,包括症状性低血糖、经确认的低血糖、重度低血糖和夜间低血糖 13. 低血糖发生率的亚组分析:按磺脲类药物(SU)使用(有/无),组内及组间进行比较 14. HbA1c < 7% 的达标率的亚组分析:以糖尿病病程、OAD 治疗持续时间、基线FPG、基线HbA1c 以及年龄等分组 15. 治疗结束时FPG 水平与HbA1c 降幅、达标率(HbA1c < 7%)以及经确认的低血糖的相关性分析 16. 药物经济学评估(HbA1c、药物费用、重度低血糖相关的医疗费用) |
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Objectives of Study: |
1. To identify a best FPG target for Chinese type 2 diabetes mellitus patients using insulin glargine which can provide the highest control rate of HbA1c< 7%; 2. The control rate of HbA1c <=6.5% achievement; 3. The control rate of HbA1c < 7.0% in patients achieving their FPG targets; 4. The percentage of patients achieving HbA1c < 7% without hypoglycemia; 5. The percentage of patients achieving the FPG target without hypoglycemia; 6. The percentage of patients achieving the FPG target and PPG target (2-hour post-breakfast <10 mmol/L); 7. The percentage of patients meeting HbA1c < 7% with FPG > 7 mmol/L, > 6.1 and ≤ 7 mmol/L, > 5.6 and ≤ 6.1 mmol/L, > 5.0 and ≤ 5.6 mmol/L, and ≤ 5 mmol/L without hypoglycemia 8. The reduction of HbA1c from the baseline 9. The reduction of FPG and PPG 10. Final insulin dose in each arm at the end of the study 11. Change in weight in each treatment arm from beginning to the end of the study 12. Rate of hypoglycemia, including symptomatic hypoglycemia, confirmed hypoglycemia, severe hypoglycemia, and nocturnal hypoglycemia 13. Subgroup analysis of hypoglycemia occurrence by the use of sulfonylurea (SU, with or without) intra-group and inter-group 14. Subgroup analysis of control rate of HbA1c < 7% by duration of diabetes, duration of OAD treatment, baseline FPG, baseline HbA1c and age 15. Analysis correlation between FPG level and HbA1c reduction, control rate (HbA1c< 7%) and confirmed hypoglycemia at end of treatment 16. Cost-effectiveness analysis (HbA1c, drug cost, medical cost related to severe hypoglycemia) |
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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. 18~65周岁 |
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Inclusion criteria |
1. Aged 18 - 65 years old; |
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排除标准: |
1. 1型糖尿病患者 |
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Exclusion criteria: |
1. Type 1 diabetes patients; |
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研究实施时间: Study execute time: |
从 From 2015-09-07 00:00:00至 To 2017-10-25 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2015-09-11 00:00:00 至 To 2017-03-11 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): |
使用中心随机化服务(IVRS/IWRS),按比例随机分入三组 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Centralized Randomization service (IVRS/IWRS) to randomized into three groups |
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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 |
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): |
暂无信息 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
NA |
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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: |
暂无信息 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
NA |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |