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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: |
2021-06-21 23:21:00 |
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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: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
陈晓莉医师:请填写伦理委员会联系人。 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: |
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: |
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: |
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: |
(1)评价滋肾育胎丸对冻融周期胚胎移植及妊娠结局的影响。 (2)应用基因组学和生物信息学分析子宫内膜细胞容受性相关基因网络,以及补肾活血法改善子宫内膜容受性的作用靶点,为中医药改善子宫内膜容受性提供科学依据,并为进一步探讨中医药在不孕症辅助生殖技术中的作用及可能的调控机制奠定基础。 (3)通过生物信息学技术可将基因组学和代谢组学得到的系统生物学指标与临床生化指标、影像学指标相关联,建立整合生物标志物评价体系,评价药效,阐述其分子调控机制。 |
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Objectives of Study: |
(1) evaluating the effect of Zishen Yutai Pill on embryo freezing and thawing cycle and pregnancy outcome; (2) To discover the endometrial cells receptivity related gene networks and the action target of invigorating kidney and promoting blood circulation therapy with the application of genomics and bioinformatics analysis, providing scientific basis of traditional Chinese medicine improving the receptivity of endometrium, and to further explore the role of TCM in assisted reproductive technology and lay the foundation of possible regulatory mechanism; (3) Using bioinformatics technology to analyze the correlation between genomics and metabolomics markers with clinical biochemical index, imaging index, to establish an integrated evaluation system of biomarkers, to evaluate drug efficacy and its molecular regulation mechanism. |
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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 2018-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2017-02-01 00:00:00 至 To 2018-12-31 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: |
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,非代谢异常组需要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: Zishenyutai pill group (placebo pills / making the same appearance and real drugs by pharmaceutical companies). 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 |