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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: |
2016-02-02 18:33:06 |
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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: |
U1111-1172-1058 |
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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2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: |
2F, 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. 评估BGStar仪器培训前患者对血糖仪操作特征的总体偏好 8. 通过问卷对BGStar仪器操作特征打分,评估BGStar培训及使用6个月后患者对BGStar使用的总体满意度 |
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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. To assess patient general preference of handling features of blood glucose monitor (BGM) device before BGStar device training; 8. To assess patient overall satisfaction with BGStar use by questionnaire to rate handling features of BGStar device after training and use of BGStar for 6 months. |
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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. 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: |
公开/Public |
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盲法: |
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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 |
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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): |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
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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: |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |