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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-INR-17010809 |
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最近更新日期: Date of Last Refreshed on: |
2021-06-30 21:57:25 |
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注册时间: Date of Registration: |
2017-03-07 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: |
补肾中成药(滋肾育胎丸)在辅助生殖冻融胚胎移植中的一项多中心,临床随机对照研究 |
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Public title: |
A multicenter, randomized, controlled clinical trial of the traditional Chinese medicine of Tonifying the kidney (Zishen yutai pills) in the assisted reproductive frozen thawed embryo transfer |
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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: |
补肾中成药(滋肾育胎丸)在辅助生殖冻融胚胎移植中的一项多中心,临床随机对照研究 |
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Scientific title: |
A multicenter, randomized, controlled clinical trial of the traditional Chinese medicine of Tonifying the kidney (Zishen yutai pills) in the assisted reproductive frozen thawed embryo transfer |
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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: |
陈晓莉 |
研究负责人: |
陈晓莉 |
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Applicant: |
Xiaoli Chen |
Study leader: |
Xiaoli Chen |
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申请注册联系人电话: Applicant telephone: |
+86 15813310709 |
研究负责人电话: Study leader's telephone: |
+86 15813310709 |
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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: |
gzxiaolichen@163.com |
研究负责人电子邮件: Study leader's E-mail: |
gzxiaolichen@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: |
广州市沿江西路107号 |
研究负责人通讯地址: |
广州市沿江西路107号 |
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Applicant address: |
107 Yanjiang Road West, Guangzhou, Guangdong, China |
Study leader's address: |
107 Yanjiang Road West, Guangzhou, Guangdong, 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: |
中山大学孙逸仙纪念医院 |
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Applicant's institution: |
Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University |
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研究负责人所在单位: |
中山大学孙逸仙纪念医院 |
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Affiliation of the Leader: |
Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University |
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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: |
2017-01-01 |
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: |
中山大学孙逸仙纪念医院生殖医学伦理委员会 |
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Name of the ethic committee: |
Reproductive Ethics Committee of Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2017-06-26 00:00:00 |
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伦理委员会联系人: |
未说明 |
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Contact Name of the ethic committee: |
Not stated |
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伦理委员会联系地址: |
广州市沿江西路107号 |
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Contact Address of the ethic committee: |
107 Yanjiang Road West, Guangzhou, Guangdong, China |
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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: |
中山大学孙逸仙纪念医院 |
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Primary sponsor: |
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University |
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研究实施负责(组长)单位地址: |
广州市沿江西路107号 |
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Primary sponsor's address: |
107 Yanjiang Road West, Guangzhou, Guangdong, 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: |
广州市科技创新委员会 |
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Source(s) of funding: |
Guangzhou Science Technology and Innovation Commission |
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Target disease: |
Infertility |
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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: |
治疗新技术临床试验 | ||||||||||||||||||||||
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Study phase: |
New Treatment Measure Clinical Study |
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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: |
通过随机对照双盲的临床试验研究,评价滋肾育胎丸对冻融周期胚胎移植及妊娠结局的影响。 |
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Objectives of Study: |
To evaluate the effects of Zishen Yutai Pills on frozen embryo transfer and pregnancy outcome through a randomized controlled double-blind clinical trial. |
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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) 取卵周期年龄≤43周岁的妇女; |
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Inclusion criteria |
1) women in egg retrieval cycle are younger than 43 years old; |
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排除标准: |
1) 患有《母婴保健法》规定的不宜生育的、目前无法进行胚胎植入前遗传学诊断的遗传性疾病者; |
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Exclusion criteria: |
1) have diseases that law on maternal and infant health care regulation suggest not to birth, or genetic diseases that currently cannot take out pre-implantation genetic diagnosis; |
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研究实施时间: Study execute time: |
从 From 2017-02-01 00:00:00至 To 2020-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2017-02-01 00:00:00 至 To 2019-08-31 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: |
正在进行 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): |
该试验设计为平行设计的随机对照双盲研究,按 1:1 等比分配设立 2 组:滋肾育胎丸组/安慰剂(由药厂制作外表与真正药物相同的药丸)。按照公式, n为需要样本数,Zα、Zβ各为α及β值对应的标准正态分布值,根据前期研究患者依从性情况,选取滋肾育胎丸组:安慰剂组=1:1,考虑脱落率=20%,确定本研究滋肾育胎丸组440例,安慰剂组需要440例。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
The experimental design was a randomized controlled double-blind study of parallel design, according to the 1:1 geometric distribution to set up 2 groups: Zishen Yutai Pills group and placebo group. According to the formula, n is the sample num |
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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: |
双盲 |
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Blinding: |
Double blind |
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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个月内公开 请说明原始数据共享的方式 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Six months after the trial |
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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: |
Epidata 数据库 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Epidata |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |