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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: |
ChiCTR2600125528 |
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最近更新日期: Date of Last Refreshed on: |
2026-05-28 08:53:26 |
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注册时间: Date of Registration: |
2026-05-28 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: |
中国人群常见弱D血型患者输注普通RhD阳性血液安全性与有效性的临床研究 |
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Public title: |
A clinical trial on the safety and efficacy of transfusing RhD-positive blood in patients with common weak D blood types in the Chinese population |
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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: |
中国人群常见弱D血型患者输注普通RhD阳性血液安全性与有效性的多中心单臂临床研究 |
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Scientific title: |
A multicenter, single-arm clinical trial on the safety and efficacy of transfusing RhD-positive blood in patients with common weak D blood types in the Chinese population |
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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: |
苑召虎 |
研究负责人: |
付涌水 |
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Applicant: |
ZhaoHu Yuan |
Study leader: |
Yongshui Fu |
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申请注册联系人电话: Applicant telephone: |
+86 20 81048643 |
研究负责人电话:
Study leader's |
+86 20 8358 6171 |
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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: |
eyyuanzhaohu@scut.edu.cn |
研究负责人电子邮件: Study leader's E-mail: |
fuyongshui@sina.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: |
广州市越秀区盘福路1号 |
研究负责人通讯地址: |
广州市越秀区盘福路1号 |
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Applicant address: |
No. 1 Panfu Road, Yuexiu District, Guangzhou, Guangdong Province, China |
Study leader's address: |
No. 1 Panfu Road, Yuexiu District, Guangzhou, Guangdong Province, China |
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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: |
广州市第一人民医院 |
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Applicant's institution: |
Guangzhou First People's Hospital |
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研究负责人所在单位: |
广州市第一人民医院 |
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Affiliation of the Leader: |
Guabgzhou First People‘s 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: |
K-2026-069-01 |
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: |
广州市第一人民医院伦理委员会 |
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Name of the ethic committee: |
Ethics committee of Guangzhou First People's Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2026-04-07 00:00:00 | ||
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伦理委员会联系人: |
罗裕 |
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Contact Name of the ethic committee: |
Luo Yu |
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伦理委员会联系地址: |
广州市越秀区盘福路1号 |
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Contact Address of the ethic committee: |
No. 1 Panfu Road, Yuexiu District, Guangzhou, Guangdong Province, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 10 81045412 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
457306297@qq.com |
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研究实施负责(组长)单位: |
广州市第一人民医院 |
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Primary sponsor: |
Guabgzhou First People‘s Hospital |
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研究实施负责(组长)单位地址: |
广州市越秀区盘福路1号 |
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Primary sponsor's address: |
No. 1 Panfu Road, Yuexiu District, Guangzhou, Guangdong 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: |
广州市医学重点学科(2025-2027年) |
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Source(s) of funding: |
The Key Medical Disciplines and Specialties Program of Guangzhou (2025-2027) |
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研究疾病: |
胎儿新生儿溶血病 |
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Target disease: |
HDFN,Hemolytic Disease of the Fetus and Newborn) |
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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: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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研究设计: |
单臂 |
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Study design: |
Single arm |
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研究目的: |
多中心大样本确证中国人群常见的弱D15、弱D960A、弱D25、弱D72和弱D33血型患者输注RhD阳性(D+)血液的安全性及有效性,为中国人群这五种常见弱D血型患者建立精准输血指南提供临床依据。 |
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Objectives of Study: |
A multicenter, large-sample study to confirm the safety and efficacy of RhD-positive (D+) blood transfusion in patients with the common weak D blood types (weak D type 15, weak D 960A, weak D type 25, weak D type 72, and weak D type 33) in the Chinese population, providing clinical evidence for establishing accurate transfusion guidelines for these five common weak D types in the Chinese population. |
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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. 18~80 周岁成年男性的弱 D 血型患者,或 49~80 周岁非育龄期女性的弱 D 血型患者; 2. 符合《临床输血技术规范》中内科、手术及创伤输血指南,结合患者的贫血程度、心肺代偿功能、有无代谢率增高以及年龄等因素,临床决定进行红细胞输注治疗的患者; 3. 试验前自愿签署临床试验输血治疗知情同意书,患者和/或其法定代理人有能力对试验内容、过程及可能出现的不良反应充分了解,并能遵守方案规定的访视及检查。 |
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Inclusion criteria |
1.Adult male weak D patients aged 18–80 years, or non-reproductive female weak D patients aged 49–80 years; |
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排除标准: |
1.既往输血有严重输血不良反应的患者; |
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Exclusion criteria: |
1.Patients with a history of severe transfusion adverse reactions; |
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研究实施时间: Study execute time: |
从 From 2026-05-31 00:00:00至 To 2028-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-05-31 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): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
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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: |
无 |
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Blinding: |
None |
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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: |
采用病例记录表进行数据采集和管理. |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Data collection and management will be performed using a Case Report Form. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |