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注册号: Registration number: |
ChiCTR2300074731 |
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最近更新日期: Date of Last Refreshed on: |
2024-01-05 23:13:05 |
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注册时间: Date of Registration: |
2023-08-15 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: |
显性单基因遗传病无创产前筛查多中心临床研究 |
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Public title: |
A multicenter clinical study on non-invasive prenatal screening for dominant monogenic genetic diseases |
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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: |
显性单基因遗传病无创产前筛查多中心临床研究 |
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Scientific title: |
A multicenter clinical study on non-invasive prenatal screening for dominant monogenic genetic diseases |
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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: |
白婷 |
研究负责人: |
刘洪倩 |
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Applicant: |
Ting Bai |
Study leader: |
Hongqian Liu |
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申请注册联系人电话: Applicant telephone: |
+86 136 6620 3645 |
研究负责人电话:
Study leader's |
+86 139 8050 2320 |
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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: |
baiting3033@163.com |
研究负责人电子邮件: Study leader's E-mail: |
hongqian.liu@163.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: |
四川省成都市武侯区人民南路三段17号 |
研究负责人通讯地址: |
四川省成都市武侯区人民南路三段17号 |
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Applicant address: |
17, Section 3, Renmin South Road, Wuhou District, Chengdu, Sichuan |
Study leader's address: |
17, Section 3, Renmin South Road, Wuhou District, Chengdu, Sichuan |
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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: |
四川大学华西第二医院 |
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Applicant's institution: |
West China Second University Hospital of Sichuan University |
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研究负责人所在单位: |
四川大学华西第二医院 |
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Affiliation of the Leader: |
West China Second University Hospital of Sichuan 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: |
医学科研2023伦审批第(082)号 |
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: |
四川大学华西第二医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of West China Second University Hospital of Sichuan University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-06-28 00:00:00 | ||
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伦理委员会联系人: |
马驰 |
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Contact Name of the ethic committee: |
Chi Ma |
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伦理委员会联系地址: |
四川省成都市武侯区人民南路三段17号 |
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Contact Address of the ethic committee: |
17, Section 3, Renmin South Road, Wuhou District, Chengdu, Sichuan |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 28 8857 0104 |
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: |
四川大学华西第二医院 |
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Primary sponsor: |
West China Second University Hospital of Sichuan University |
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研究实施负责(组长)单位地址: |
四川省成都市武侯区人民南路三段17号 |
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Primary sponsor's address: |
17, Section 3, Renmin South Road, Wuhou District, Chengdu, Sichuan |
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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: |
国家重点研发计划重点专项(2022YFC2703400) |
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Source(s) of funding: |
National key research and development program (2022YFC2703400) |
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研究疾病: |
显性单基因遗传病 |
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Target disease: |
Dominant monogenic genetic diseases |
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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: |
诊断试验 |
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Study type: |
Diagnostic test |
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研究所处阶段: |
诊断试验新技术临床试验 | ||||||||||||||||||||||
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Study phase: |
Diagnostic New Technique Clincal Study |
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研究设计: |
诊断试验诊断准确性 |
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Study design: |
Diagnostic test for accuracy |
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研究目的: |
针对中国围产期胎儿自发产生的显性遗传变异导致的单基因遗传病,目前还没有精准的产前筛查方法这一临床问题,本项目拟开发基于基因捕获技术和分子标签技术的胎儿自发显性单基因遗传病无创产前筛查新技术,同时通过多中心临床研究,建立胎儿自发显性单基因遗传病的无创产前筛查临床应用路径,筑牢显性单基因遗传病出生缺陷防控体系,有效降低严重出生缺陷。 |
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Objectives of Study: |
Currently, there is no precise prenatal screening method for single gene genetic diseases caused by spontaneous dominant genetic variations for perinatal fetuses in China. Our study plans to develop a new non-invasive prenatal screening technology for fetal spontaneous dominant single gene genetic diseases based on gene capture technology and molecular labeling technology. At the same time, to establishing a non-invasive prenatal screening clinical application pathway for fetal spontaneous dominant monogenic genetic diseases through multicenter clinical research, and to strengthen the prevention system for birth defects in dominant monogenic genetic diseases to reduce severe birth defects effectively. |
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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: |
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Inclusion criteria |
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排除标准: |
1.未成年孕妇; 2.孕周<12+0周; 3. 1年内接受过异体输血、器官移植或细胞治疗; 4.孕期母体恶性肿瘤; 5.孕妇本人为显性单基因遗传病患者; 6. 医师认为有明显影响结果准确性的其他情形。 |
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Exclusion criteria: |
1. Underage pregnant women; 2. Pregnancy<12+0 weeks; 3. Received allogeneic blood transfusion, organ transplantation, or cell therapy within one year; 4. Maternal malignant tumors during pregnancy; 5. The pregnant woman herself is a patient with a dominant monogenic genetic disease; 6. Other situations that the physician believes have a significant impact on the accuracy of the results. |
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研究实施时间: Study execute time: |
从 From 2023-04-23 00:00:00至 To 2028-04-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-08-21 00:00:00 至 To 2028-04-30 00:00:00 |
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诊断试验: Diagnostic Tests: |
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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: |
女性 |
Gender: |
Female |
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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: |
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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): |
暂未确定。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Not yet. |
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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: |
暂未确定。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Not yet. |
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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 |