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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: |
ChiCTR2000037511 |
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最近更新日期: Date of Last Refreshed on: |
2020-08-28 12:18:36 |
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注册时间: Date of Registration: |
2020-08-28 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: |
静脉注射丙种球蛋白对复发性流产合并抗磷脂综合征疗效评价的多中心临床研究 |
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Public title: |
The effect of intravenous immunoglobulin on pregnancy outcomes of recurrent spontaneous abortion combined with antiphospholipid syndrome:a multi-center clinical trial |
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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: |
静脉注射丙种球蛋白对复发性流产合并抗磷脂综合症治疗效果的多中心临床研究 |
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Scientific title: |
The effect of intravenous immunoglobulin on pregnancy outcomes of recurrent spontaneous abortion combined with antiphospholipid syndrome:a multi-center clinical trial |
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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: |
赵岩 |
研究负责人: |
金莉萍 |
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Applicant: |
Zhao Yan |
Study leader: |
Liping Jin |
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申请注册联系人电话: Applicant telephone: |
13636573676 |
研究负责人电话: Study leader's telephone: |
18918779150 |
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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: |
zy861201@163.com |
研究负责人电子邮件: Study leader's E-mail: |
jinlp01@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: |
上海市高科西路2699号 |
研究负责人通讯地址: |
上海市高科西路2699号 |
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Applicant address: |
NO. 2699, Gaoke Road, Shanghai |
Study leader's address: |
NO. 2699, Gaoke Road, Shanghai |
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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: |
上海市第一妇婴保健院 |
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Applicant's institution: |
Shanghai First Maternity and Infant Hospital |
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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/Yes |
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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: |
KS20292 |
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: |
上海市第一妇婴保健院 |
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Name of the ethic committee: |
Shanghai First Maternity and Infant Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
1990-01-01 00:00:00 |
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伦理委员会联系人: |
罗烨 |
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Contact Name of the ethic committee: |
Ye Luo |
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伦理委员会联系地址: |
上海市浦东新区高科西路2699号 |
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Contact Address of the ethic committee: |
NO. 2699, Gaoke Road, Shanghai |
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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: |
上海市第一妇婴保健院 |
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Primary sponsor: |
Shanghai First Maternity and Infant Hospital |
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研究实施负责(组长)单位地址: |
上海市浦东新区高科西路2699号 |
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Primary sponsor's address: |
NO. 2699, Gaoke Road, Shanghai |
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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: |
上海申康医院发展中心 |
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Source(s) of funding: |
Hospital development center |
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Target disease: |
recurrent spontaneous abortion |
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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: |
I期临床试验 | ||||||||||||||||||||||
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Study phase: |
1 |
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研究设计: |
横断面 |
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Study design: |
Cross-sectional |
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研究目的: |
明确静脉注射丙种球蛋白对复发性流产合并抗磷脂综合症妊娠结局的影响,形成针对复发性流产合并抗磷脂综合症患者的个体化治疗方案。 |
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Objectives of Study: |
This project aims to illustrate the prognosis of intravenous immunoglobulin on pregnancy outcomes of recurrent spontaneous abortion combined with antiphospholipid syndromeand to form a individualized therapeutic plan。 |
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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: |
【纳入标准】 |
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Inclusion criteria |
Patients who (are) |
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排除标准: |
1. 若纳入试验后受试者发生流产,行胚胎染色体检查证实为染色体异常者; |
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Exclusion criteria: |
Patients who (are) |
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研究实施时间: Study execute time: |
从 From 2020-10-01 00:00:00至 To 2022-09-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2020-12-01 00:00:00 至 To 2022-06-30 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: |
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): |
PGT实验室人员根据计算机生成的随机数字分配患者 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
The full-time PGT employee randomized this patients into one of the two groups by computor-generated random numbers |
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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 |
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): |
试验完成后6个月原始数据上传至注册网站共享原始数据 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
6 month after the trial complete upload the raw data to this website |
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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: |
病历记录表由参与本试验的临床医生采集及管理,最终汇总给本项目负责人。本中心有专门的电子病历系统,由专人管理。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF is managed by the investigators who take part in this trial, the person in charg will collect these CRFs. There is electronic medical record systerm in our center which is managed by designated person. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |