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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: |
ChiCTR2600118638 |
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最近更新日期: Date of Last Refreshed on: |
2026-04-16 14:27:43 |
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注册时间: Date of Registration: |
2026-02-09 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: |
评价通络明目胶囊治疗非增生期糖尿病视网膜病变有效性和安全性的多中心、随机、双盲、安慰剂对照临床研究 |
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Public title: |
A multicenter, randomized, double-blind, placebo-controlled clinical study to evaluate the efficacy and safety of Tongluo Mingmu Capsules in the treatment of non-proliferative diabetic retinopathy |
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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: |
评价通络明目胶囊治疗非增生期糖尿病视网膜病变有效性和安全性的多中心、随机、双盲、安慰剂对照临床研究 |
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Scientific title: |
A multicenter, randomized, double-blind, placebo-controlled clinical study to evaluate the efficacy and safety of Tongluo Mingmu Capsules in the treatment of non-proliferative diabetic retinopathy |
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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: |
匡洪宇 |
研究负责人: |
匡洪宇 |
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Applicant: |
Hongyu Kuang |
Study leader: |
Kuang Hongyyu |
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申请注册联系人电话: Applicant telephone: |
+86 13895751367 |
研究负责人电话:
Study leader's |
+86 451 8555 2350 |
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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: |
1640699950@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
ydykuanghongyu@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: |
哈尔滨医科大学附属第一医院内分泌科 |
研究负责人通讯地址: |
黑龙江省哈尔滨市南岗区邮政街23号 |
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Applicant address: |
Department of Endocrinology, the First Affiliated Hospital of Harbin Medical University |
Study leader's address: |
No. 23, Post Street, Nangang District, Harbin, Heilongjiang Province |
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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: |
哈尔滨医科大学附属第一医院 |
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Applicant's institution: |
The First Affiliated Hospital of Harbin Medical University |
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研究负责人所在单位: |
哈尔滨医科大学附属第一医院 |
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Affiliation of the Leader: |
The First Affiliated Hospital of Harbin Medical University |
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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: |
2025349 |
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: |
哈尔滨医科大学附属第一医院伦理委员会 |
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Name of the ethic committee: |
The Ethics Committee of the First Affiliated Hospital of Harbin Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-09-17 00:00:00 | ||
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伦理委员会联系人: |
鲍美汐 |
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Contact Name of the ethic committee: |
Bao MeiXi |
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伦理委员会联系地址: |
黑龙江省哈尔滨市南岗区邮政街23号 |
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Contact Address of the ethic committee: |
No. 23, Post Street, Nangang District, Harbin, Heilongjiang Province |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 451 85552350 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
black9090@163.com |
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研究实施负责(组长)单位: |
哈尔滨医科大学附属第一医院 |
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Primary sponsor: |
The First Affiliated Hospital of Harbin Medical University |
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研究实施负责(组长)单位地址: |
黑龙江省哈尔滨市南岗区邮政街23号 |
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Primary sponsor's address: |
No. 23, Post Street, Nangang District, Harbin, Heilongjiang Province |
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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: |
石家庄以岭药业股份有限公司 |
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Source(s) of funding: |
Shijiazhuang Yiling Pharmaceutical Co., Ltd. |
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研究疾病: |
非增生期糖尿病视网膜病变 |
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Target disease: |
Non-Proliferative Diabetic Retinopathy |
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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: |
上市后药物 | ||||||||||||||||||||||
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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: |
评价通络明目治疗非增生期糖尿病视网膜病变的有效性和安全性。 |
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Objectives of Study: |
Evaluate the efficacy and safety of Tongluo Mingmu therapy in treating non-proliferative diabetic retinopathy. |
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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:18-70岁(包含两端值); |
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Inclusion criteria |
1.Age: 18-70 years (inclusive); |
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排除标准: |
1. 糖化血红蛋白(HbA1c)水平> 8%; 2. 曾接受过视网膜激光光凝治疗或适合光凝治疗者; 3. 规律服用降压药物后血压仍大于160/100mmHg者; 4. 12周内使用治疗DR以及改善微循环的药物; 5. 患有其他眼部疾病,如青光眼、白内障、非糖尿病性视网膜病变、葡萄膜炎、视网膜脱离、视神经疾病或高度近视; 6. 肝或肾功能损害符合以下情况之一的:丙氨酸氨基转移酶(ALT)、天门冬氨酸氨基转移酶(AST)、总胆红素(TBIL)以及碱性磷酸酶(ALP)>2.0×ULN,血肌酐(Cr)>2.0×ULN、尿素氮(BUN)/尿素(UREA)>2.0×ULN; 7. 血脂情况符合下列之一的:总胆固醇>2.0×ULN,低密度脂蛋白胆固醇>2.0×ULN,甘油三酯>2.0×ULN; 8. .患有严重精神或心理疾病者; 9. 孕妇、计划怀孕或哺乳期妇女; 10. 对试验药物成份过敏者; 11. 在过去三个月内参加过其他临床试验; 12. 研究者认为受试者有潜在风险或其它因素不适宜参加本试验者; |
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Exclusion criteria: |
1.Glycated hemoglobin (HbA1c) level > 8%; |
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研究实施时间: Study execute time: |
从 From 2025-09-01 00:00:00至 To 2027-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-03-01 00:00:00 至 To 2027-12-31 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: |
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): |
由研究者通过中央随机系统分组 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Grouped by researchers through a central randomization system. |
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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: |
受试者和研究者双方都不知道受试者被分配到了哪个组别。 |
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Blinding: |
Both the subjects and the researchers do not know which group the subjects have been assigned to. |
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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): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
None |
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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: |
病例记录表 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Report Form |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |